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44164

Beschrijving

Study ID: 101468/205 Clinical Study ID: 101468/205 Study Title:A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00197080 Sponsor: GlaxoSmithKline Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome

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Versies (2)
  1. 07-02-19 07-02-19 -
  2. 20-09-21 20-09-21 -
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GlaxoSmithKline

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20 september 2021

DOI

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Creative Commons BY-NC 3.0
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    Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome NCT00197080

    Engels

    Screening - Eligibility Question

    1 Formulieren  
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI-1
    C1512693
    1. Subjects diagnosed with RLS using the RLS Diagnostic Clinical Interview and the International RLS Study Group (IRLSSG) Diagnostic Criteria at the Screening Visit.
    Beschrijving

    1. Subjects diagnosed with RLS using the RLS Diagnostic Clinical Interview and the International RLS Study Group (IRLSSG) Diagnostic Criteria at the Screening Visit.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0035258
    UMLS CUI [2,1]
    C1537061
    UMLS CUI [2,2]
    C0035258
    2. Subjects > 18 years and < 80 years of age.
    Beschrijving

    2. Subjects > 18 years and < 80 years of age

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    3. Subjects have had RLS symptoms with a history of a minimum of 20 evening and nights of RLS episodes during the month prior to the Screening Visit (e.g., any combination of evenings and/or nights for >20 days). In the case of a subject currently receiving medication for the treatment of RLS at the Screening Visit, this inclusion criterion can be waived. However, the subject must discontinue and washout any previous medication for the treatment of RLS or sleep prior to the Baseline Visit (Day 0). The minimum discontinuation period for washout is generally 5 half-lives of the medication or 7 consecutive nights medication-free prior to baseline, whichever is the longer period.
    Beschrijving

    3. Restless Legs Syndrome; Frequencies (time pattern) | Restless Legs Syndrome; Pharmaceutical Preparations; Washout Period

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0035258
    UMLS CUI [1,2]
    C0439603
    UMLS CUI [2,1]
    C0035258
    UMLS CUI [2,2]
    C0013227
    UMLS CUI [2,3]
    C1710661
    4. Subjects must be experiencing RLS symptoms requiring treatment prior to bedtime, but no earlier than 5:00 PM.
    Beschrijving

    4. Subjects must be experiencing RLS symptoms requiring treatment prior to bedtime, but no earlier than 5:00 PM.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0035258
    UMLS CUI [1,2]
    C0087111
    UMLS CUI [1,3]
    C0521112
    UMLS CUI [1,4]
    C0332152
    5. Subjects must have given written informed consent prior to any specific study procedures.
    Beschrijving

    5. Subjects must have given written informed consent prior to any specific study procedures.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion criteria
    Beschrijving

    Exclusion criteria

    Alias
    UMLS CUI-1
    C0680251
    1. Subjects requiring treatment of daytime RLS symptoms (daytime defined as 7:00 AM until 5:00 PM).
    Beschrijving

    1. Subjects requiring treatment of daytime RLS symptoms (daytime defined as 7:00 AM until 5:00 PM).

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0035258
    UMLS CUI [1,2]
    C0087111
    UMLS CUI [1,3]
    C1457887
    UMLS CUI [1,4]
    C0332169
    2. Signs of secondary RLS (e.g. end stage renal disease, iron deficient anemia or pregnancy at Baseline Visit).
    Beschrijving

    2. Signs of secondary RLS (e.g. end stage renal disease, iron deficient anemia or pregnancy at Baseline Visit).

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1261469
    UMLS CUI [2]
    C0022661
    UMLS CUI [3]
    C0162316
    UMLS CUI [4]
    C0032961
    3. Subjects with a serum ferritin level of < 10 mcg/L (ng/mL) that has not resolved by the time of the Baseline Visit.
    Beschrijving

    3. Subjects with a serum ferritin level of < 10 mcg/L (ng/mL) that has not resolved by the time of the Baseline Visit.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0696113
    4. Subjects having a clinically significant abnormal lab, ECG, or physical exam findings not resolved by time of baseline examinations. Abnormal 12-lead ECG findings include, but are not limited to the following: myocardial ischemia, clinically significant conduction abnormalities, or clinically significant arrhythmias
    Beschrijving

    Laboratory test result abnormal; Clinical Significance | Electrocardiogram abnormal; Clinical Significance | Physical Examination; Abnormal; Clinical Significance | Myocardial Ischemia | Abnormal cardiac conduction; Clinical Significance | Cardiac Arrhythmia; Clinical Significance

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0438215
    UMLS CUI [1,2]
    C2826293
    UMLS CUI [2,1]
    C0522055
    UMLS CUI [2,2]
    C2826293
    UMLS CUI [3,1]
    C0031809
    UMLS CUI [3,2]
    C0205161
    UMLS CUI [3,3]
    C2826293
    UMLS CUI [4]
    C0151744
    UMLS CUI [5,1]
    C0232219
    UMLS CUI [5,2]
    C2826293
    UMLS CUI [6,1]
    C0003811
    UMLS CUI [6,2]
    C2826293
    5. Subjects who suffer from a primary sleep disorder other than RLS that may significantly affect the symptoms of RLS (e.g. narcolepsy, sleep terror disorder, sleepwalking disorder, breathing related sleep disorder).
    Beschrijving

    5. Subjects who suffer from a primary sleep disorder other than RLS that may significantly affect the symptoms of RLS (e.g. narcolepsy, sleep terror disorder, sleepwalking disorder, breathing related sleep disorder).

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0236991
    UMLS CUI [1,2]
    C0035258
    UMLS CUI [1,3]
    C0205394
    UMLS CUI [2,1]
    C0035258
    UMLS CUI [2,2]
    C1457887
    UMLS CUI [3]
    C0027404
    UMLS CUI [4,1]
    C0851578
    UMLS CUI [4,2]
    C0037320
    UMLS CUI [5]
    C0037672
    UMLS CUI [6]
    C0236845
    6. Subjects diagnosed with movement disorders (e.g. Parkinson’s Disease, dyskinesias, and dystonias).
    Beschrijving

    6. Subjects diagnosed with movement disorders (e.g. Parkinson’s Disease, dyskinesias, and dystonias).

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0026650
    UMLS CUI [2]
    C0030567
    UMLS CUI [3]
    C0013384
    UMLS CUI [4]
    C0013421
    7. Subjects who have medical conditions which, in the opinion of the investigator, could affect efficacy assessments or clinically significant or unstable medical conditions that present a safety concern. These may include, but are not limited to the following disorders: diabetes, peripheral neuropathy, rheumatoid arthritis, fibromyalgia syndrome, symptomatic orthostatic hypotension, severe cardiovascular disease, hepatic or renal failure, pleuro-pulmonary fibrosis).
    Beschrijving

    7. Subjects who have medical conditions which, in the opinion of the investigator, could affect efficacy assessments or clinically significant or unstable medical conditions that present a safety concern.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0012634
    UMLS CUI [1,2]
    C1280519
    UMLS CUI [1,3]
    C0220825
    UMLS CUI [2,1]
    C0012634
    UMLS CUI [2,2]
    C0443343
    UMLS CUI [2,3]
    C0036043
    UMLS CUI [2,4]
    C2699424
    UMLS CUI [3]
    C0011849
    UMLS CUI [4]
    C0031117
    UMLS CUI [5]
    C0003873
    UMLS CUI [6]
    C0016053
    UMLS CUI [7]
    C0740482
    UMLS CUI [8,1]
    C0007222
    UMLS CUI [8,2]
    C0205082
    UMLS CUI [9]
    C0035078
    UMLS CUI [10]
    C0085605
    UMLS CUI [11]
    C0034069
    8. Subjects with a history of alcohol or substance abuse within the past year.
    Beschrijving

    8. Subjects with a history of alcohol or substance abuse within the past year.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0085762
    UMLS CUI [1,2]
    C1299544
    9. Subjects with a diastolic blood pressure >110mmHg or <50mmHg or systolic blood pressure > 180mmHg or <90mmHg at the Screening or Baseline Visit.
    Beschrijving

    9. Subjects with a diastolic blood pressure >110mmHg or <50mmHg or systolic blood pressure > 180mmHg or <90mmHg at the Screening or Baseline Visit.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0428883
    UMLS CUI [2]
    C0871470
    10. Subjects taking any medication known to induce drowsiness, affect RLS or sleep and that have not been discontinued prior to the Baseline Visit. These medications include the following: • antidepressants (tricyclic antidepressants, noradrenaline [norepinephrine]/ serotonin re-uptake inhibitors, selective serotonin re-uptake inhibitors, bupropion), anticonvulsants, opioids (including propoxyphene and oxycodone), anxiolytics, all sedatives/hypnotics (including benzodiazepines), lithium, oral neuroleptics, stimulants (including methylphenidate), antipsychotics, dopamine agonists, dopamine antagonists, clonidine, and sedating antihistamines (e.g. chlorpheniramine, diphenhydramine, hydroxyzine) or any preparations containing these
    Beschrijving

    10. Subjects taking any medication known to induce drowsiness, affect RLS or sleep and that have not been discontinued prior to the Baseline Visit.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0013144
    UMLS CUI [1,3]
    C0035258
    UMLS CUI [1,4]
    C0392760
    UMLS CUI [1,5]
    C0013227
    UMLS CUI [1,6]
    C0013144
    UMLS CUI [1,7]
    C0035258
    UMLS CUI [1,8]
    C0037313
    UMLS CUI [1,9]
    C0457454
    UMLS CUI [2]
    C0003290
    UMLS CUI [3]
    C0162758
    UMLS CUI [4]
    C0003286
    UMLS CUI [5,1]
    C0242402
    UMLS CUI [5,2]
    C0033493
    UMLS CUI [5,3]
    C0030049
    UMLS CUI [6]
    C0040616
    UMLS CUI [7,1]
    C0020592
    UMLS CUI [7,2]
    C0005064
    UMLS CUI [8]
    C0023870
    UMLS CUI [9,1]
    C0040615
    UMLS CUI [9,2]
    C0442027
    UMLS CUI [10,1]
    C0304402
    UMLS CUI [10,2]
    C0025810
    UMLS CUI [11]
    C0040615
    UMLS CUI [12]
    C0178601
    UMLS CUI [13]
    C0242702
    UMLS CUI [14]
    C0009014
    UMLS CUI [15,1]
    C1955826
    UMLS CUI [15,2]
    C0008281
    UMLS CUI [15,3]
    C0012522
    UMLS CUI [15,4]
    C0020404
    11. Withdrawal, introduction, or change in dose of hormone replacement therapy (HRT) and/or any drug known to substantially inhibit CYP1A2 (e.g. ciprofloxacin, cimetidine, fluvoxamine, HRT) or induce CYP1A2 (e.g. tobacco, omeprazole) within 7 days prior to Baseline Visit. Subjects already on these agents may be enrolled, but must remain on stable doses of the agents from 7 days prior to Baseline Visit through to the follow-up visit at end of study.
    Beschrijving

    11. Withdrawal, introduction, or change in dose of hormone replacement therapy (HRT) and/or any drug known to substantially inhibit CYP1A2 (e.g. ciprofloxacin, cimetidine, fluvoxamine, HRT) or induce CYP1A2 (e.g. tobacco, omeprazole) within 7 days prior to Baseline Visit.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0282402
    UMLS CUI [1,2]
    C2349954
    UMLS CUI [2,1]
    C0282402
    UMLS CUI [2,2]
    C0579004
    UMLS CUI [3,1]
    C0282402
    UMLS CUI [3,2]
    C1707811
    UMLS CUI [4,1]
    C1827504
    UMLS CUI [4,2]
    C0008809
    UMLS CUI [4,3]
    C0008783
    UMLS CUI [4,4]
    C0085228
    UMLS CUI [4,5]
    C0282402
    UMLS CUI [5,1]
    C1827490
    UMLS CUI [5,2]
    C0543414
    UMLS CUI [5,3]
    C0028978
    12. Night workers or any others whose sleeping habits are incompatible with the study design, or who would be required to make significant changes to their bedtime during the course of the study.
    Beschrijving

    12. Night workers or any others whose sleeping habits are incompatible with the study design, or who would be required to make significant changes to their bedtime during the course of the study.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0555008
    UMLS CUI [2,1]
    C0547101
    UMLS CUI [2,2]
    C4698019
    UMLS CUI [2,3]
    C0035171
    UMLS CUI [3,1]
    C0547101
    UMLS CUI [3,2]
    C4698019
    UMLS CUI [3,3]
    C0680104
    13. Subjects who have exhibited intolerance to ropinirole or any other dopamine agonist.
    Beschrijving

    13. Subjects who have exhibited intolerance to ropinirole or any other dopamine agonist.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1744706
    UMLS CUI [1,2]
    C0244821
    UMLS CUI [2,1]
    C1744706
    UMLS CUI [2,2]
    C0178601
    14. Participation in any clinical drug or device trial in the one month prior to the Baseline Visit.
    Beschrijving

    14. Participation in any clinical drug or device trial in the one month prior to the Baseline Visit.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    15. Subjects who, in the opinion of the investigator, would be non-compliant with the visit schedule or other study procedures.
    Beschrijving

    15. Subjects non-compliant with the visit schedule or other study procedures.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C2348563
    16. Women who have a positive pregnancy test or who are lactating.
    Beschrijving

    16. Women who have a positive pregnancy test or who are lactating.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C2828358
    17. Women of child-bearing potential who are not practicing a clinically accepted method of contraception such as oral contraception, surgical sterilization, IUD, diaphragm in conjunction with spermicidal foam and condom on the male partner, or systemic contraception (e.g. Norplant).
    Beschrijving

    17. Women of child-bearing potential who are not practicing a clinically accepted method of contraception.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1960468
    UMLS CUI [2,1]
    C0700589
    UMLS CUI [2,2]
    C3176353
    UMLS CUI [3]
    C0029151
    UMLS CUI [4]
    C0015787
    UMLS CUI [5]
    C0021900
    UMLS CUI [6,1]
    C0042241
    UMLS CUI [6,2]
    C3843423
    UMLS CUI [6,3]
    C0009653
    UMLS CUI [7,1]
    C0700589
    UMLS CUI [7,2]
    C1515119
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    Similar models

    Screening - Eligibility Question

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Inclusion Criteria
    C1512693 (UMLS CUI-1)
    1. Subjects diagnosed with RLS using the RLS Diagnostic Clinical Interview and the International RLS Study Group (IRLSSG) Diagnostic Criteria at the Screening Visit.
    Item
    1. Subjects diagnosed with RLS using the RLS Diagnostic Clinical Interview and the International RLS Study Group (IRLSSG) Diagnostic Criteria at the Screening Visit.
    boolean
    C0035258 (UMLS CUI [1])
    C1537061 (UMLS CUI [2,1])
    C0035258 (UMLS CUI [2,2])
    2. Subjects > 18 years and < 80 years of age
    Item
    2. Subjects > 18 years and < 80 years of age.
    boolean
    C0001779 (UMLS CUI [1])
    3. Restless Legs Syndrome; Frequencies (time pattern) | Restless Legs Syndrome; Pharmaceutical Preparations; Washout Period
    Item
    3. Subjects have had RLS symptoms with a history of a minimum of 20 evening and nights of RLS episodes during the month prior to the Screening Visit (e.g., any combination of evenings and/or nights for >20 days). In the case of a subject currently receiving medication for the treatment of RLS at the Screening Visit, this inclusion criterion can be waived. However, the subject must discontinue and washout any previous medication for the treatment of RLS or sleep prior to the Baseline Visit (Day 0). The minimum discontinuation period for washout is generally 5 half-lives of the medication or 7 consecutive nights medication-free prior to baseline, whichever is the longer period.
    boolean
    C0035258 (UMLS CUI [1,1])
    C0439603 (UMLS CUI [1,2])
    C0035258 (UMLS CUI [2,1])
    C0013227 (UMLS CUI [2,2])
    C1710661 (UMLS CUI [2,3])
    4. Subjects must be experiencing RLS symptoms requiring treatment prior to bedtime, but no earlier than 5:00 PM.
    Item
    4. Subjects must be experiencing RLS symptoms requiring treatment prior to bedtime, but no earlier than 5:00 PM.
    boolean
    C0035258 (UMLS CUI [1,1])
    C0087111 (UMLS CUI [1,2])
    C0521112 (UMLS CUI [1,3])
    C0332152 (UMLS CUI [1,4])
    5. Subjects must have given written informed consent prior to any specific study procedures.
    Item
    5. Subjects must have given written informed consent prior to any specific study procedures.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    Exclusion criteria
    C0680251 (UMLS CUI-1)
    1. Subjects requiring treatment of daytime RLS symptoms (daytime defined as 7:00 AM until 5:00 PM).
    Item
    1. Subjects requiring treatment of daytime RLS symptoms (daytime defined as 7:00 AM until 5:00 PM).
    boolean
    C0035258 (UMLS CUI [1,1])
    C0087111 (UMLS CUI [1,2])
    C1457887 (UMLS CUI [1,3])
    C0332169 (UMLS CUI [1,4])
    2. Signs of secondary RLS (e.g. end stage renal disease, iron deficient anemia or pregnancy at Baseline Visit).
    Item
    2. Signs of secondary RLS (e.g. end stage renal disease, iron deficient anemia or pregnancy at Baseline Visit).
    boolean
    C1261469 (UMLS CUI [1])
    C0022661 (UMLS CUI [2])
    C0162316 (UMLS CUI [3])
    C0032961 (UMLS CUI [4])
    3. Subjects with a serum ferritin level of < 10 mcg/L (ng/mL) that has not resolved by the time of the Baseline Visit.
    Item
    3. Subjects with a serum ferritin level of < 10 mcg/L (ng/mL) that has not resolved by the time of the Baseline Visit.
    boolean
    C0696113 (UMLS CUI [1])
    Laboratory test result abnormal; Clinical Significance | Electrocardiogram abnormal; Clinical Significance | Physical Examination; Abnormal; Clinical Significance | Myocardial Ischemia | Abnormal cardiac conduction; Clinical Significance | Cardiac Arrhythmia; Clinical Significance
    Item
    4. Subjects having a clinically significant abnormal lab, ECG, or physical exam findings not resolved by time of baseline examinations. Abnormal 12-lead ECG findings include, but are not limited to the following: myocardial ischemia, clinically significant conduction abnormalities, or clinically significant arrhythmias
    boolean
    C0438215 (UMLS CUI [1,1])
    C2826293 (UMLS CUI [1,2])
    C0522055 (UMLS CUI [2,1])
    C2826293 (UMLS CUI [2,2])
    C0031809 (UMLS CUI [3,1])
    C0205161 (UMLS CUI [3,2])
    C2826293 (UMLS CUI [3,3])
    C0151744 (UMLS CUI [4])
    C0232219 (UMLS CUI [5,1])
    C2826293 (UMLS CUI [5,2])
    C0003811 (UMLS CUI [6,1])
    C2826293 (UMLS CUI [6,2])
    5. Subjects who suffer from a primary sleep disorder other than RLS that may significantly affect the symptoms of RLS (e.g. narcolepsy, sleep terror disorder, sleepwalking disorder, breathing related sleep disorder).
    Item
    5. Subjects who suffer from a primary sleep disorder other than RLS that may significantly affect the symptoms of RLS (e.g. narcolepsy, sleep terror disorder, sleepwalking disorder, breathing related sleep disorder).
    boolean
    C0236991 (UMLS CUI [1,1])
    C0035258 (UMLS CUI [1,2])
    C0205394 (UMLS CUI [1,3])
    C0035258 (UMLS CUI [2,1])
    C1457887 (UMLS CUI [2,2])
    C0027404 (UMLS CUI [3])
    C0851578 (UMLS CUI [4,1])
    C0037320 (UMLS CUI [4,2])
    C0037672 (UMLS CUI [5])
    C0236845 (UMLS CUI [6])
    6. Subjects diagnosed with movement disorders (e.g. Parkinson’s Disease, dyskinesias, and dystonias).
    Item
    6. Subjects diagnosed with movement disorders (e.g. Parkinson’s Disease, dyskinesias, and dystonias).
    boolean
    C0026650 (UMLS CUI [1])
    C0030567 (UMLS CUI [2])
    C0013384 (UMLS CUI [3])
    C0013421 (UMLS CUI [4])
    7. Subjects who have medical conditions which, in the opinion of the investigator, could affect efficacy assessments or clinically significant or unstable medical conditions that present a safety concern.
    Item
    7. Subjects who have medical conditions which, in the opinion of the investigator, could affect efficacy assessments or clinically significant or unstable medical conditions that present a safety concern. These may include, but are not limited to the following disorders: diabetes, peripheral neuropathy, rheumatoid arthritis, fibromyalgia syndrome, symptomatic orthostatic hypotension, severe cardiovascular disease, hepatic or renal failure, pleuro-pulmonary fibrosis).
    boolean
    C0012634 (UMLS CUI [1,1])
    C1280519 (UMLS CUI [1,2])
    C0220825 (UMLS CUI [1,3])
    C0012634 (UMLS CUI [2,1])
    C0443343 (UMLS CUI [2,2])
    C0036043 (UMLS CUI [2,3])
    C2699424 (UMLS CUI [2,4])
    C0011849 (UMLS CUI [3])
    C0031117 (UMLS CUI [4])
    C0003873 (UMLS CUI [5])
    C0016053 (UMLS CUI [6])
    C0740482 (UMLS CUI [7])
    C0007222 (UMLS CUI [8,1])
    C0205082 (UMLS CUI [8,2])
    C0035078 (UMLS CUI [9])
    C0085605 (UMLS CUI [10])
    C0034069 (UMLS CUI [11])
    8. Subjects with a history of alcohol or substance abuse within the past year.
    Item
    8. Subjects with a history of alcohol or substance abuse within the past year.
    boolean
    C0085762 (UMLS CUI [1,1])
    C1299544 (UMLS CUI [1,2])
    9. Subjects with a diastolic blood pressure >110mmHg or <50mmHg or systolic blood pressure > 180mmHg or <90mmHg at the Screening or Baseline Visit.
    Item
    9. Subjects with a diastolic blood pressure >110mmHg or <50mmHg or systolic blood pressure > 180mmHg or <90mmHg at the Screening or Baseline Visit.
    boolean
    C0428883 (UMLS CUI [1])
    C0871470 (UMLS CUI [2])
    10. Subjects taking any medication known to induce drowsiness, affect RLS or sleep and that have not been discontinued prior to the Baseline Visit.
    Item
    10. Subjects taking any medication known to induce drowsiness, affect RLS or sleep and that have not been discontinued prior to the Baseline Visit. These medications include the following: • antidepressants (tricyclic antidepressants, noradrenaline [norepinephrine]/ serotonin re-uptake inhibitors, selective serotonin re-uptake inhibitors, bupropion), anticonvulsants, opioids (including propoxyphene and oxycodone), anxiolytics, all sedatives/hypnotics (including benzodiazepines), lithium, oral neuroleptics, stimulants (including methylphenidate), antipsychotics, dopamine agonists, dopamine antagonists, clonidine, and sedating antihistamines (e.g. chlorpheniramine, diphenhydramine, hydroxyzine) or any preparations containing these
    boolean
    C0013227 (UMLS CUI [1,1])
    C0013144 (UMLS CUI [1,2])
    C0035258 (UMLS CUI [1,3])
    C0392760 (UMLS CUI [1,4])
    C0013227 (UMLS CUI [1,5])
    C0013144 (UMLS CUI [1,6])
    C0035258 (UMLS CUI [1,7])
    C0037313 (UMLS CUI [1,8])
    C0457454 (UMLS CUI [1,9])
    C0003290 (UMLS CUI [2])
    C0162758 (UMLS CUI [3])
    C0003286 (UMLS CUI [4])
    C0242402 (UMLS CUI [5,1])
    C0033493 (UMLS CUI [5,2])
    C0030049 (UMLS CUI [5,3])
    C0040616 (UMLS CUI [6])
    C0020592 (UMLS CUI [7,1])
    C0005064 (UMLS CUI [7,2])
    C0023870 (UMLS CUI [8])
    C0040615 (UMLS CUI [9,1])
    C0442027 (UMLS CUI [9,2])
    C0304402 (UMLS CUI [10,1])
    C0025810 (UMLS CUI [10,2])
    C0040615 (UMLS CUI [11])
    C0178601 (UMLS CUI [12])
    C0242702 (UMLS CUI [13])
    C0009014 (UMLS CUI [14])
    C1955826 (UMLS CUI [15,1])
    C0008281 (UMLS CUI [15,2])
    C0012522 (UMLS CUI [15,3])
    C0020404 (UMLS CUI [15,4])
    11. Withdrawal, introduction, or change in dose of hormone replacement therapy (HRT) and/or any drug known to substantially inhibit CYP1A2 (e.g. ciprofloxacin, cimetidine, fluvoxamine, HRT) or induce CYP1A2 (e.g. tobacco, omeprazole) within 7 days prior to Baseline Visit.
    Item
    11. Withdrawal, introduction, or change in dose of hormone replacement therapy (HRT) and/or any drug known to substantially inhibit CYP1A2 (e.g. ciprofloxacin, cimetidine, fluvoxamine, HRT) or induce CYP1A2 (e.g. tobacco, omeprazole) within 7 days prior to Baseline Visit. Subjects already on these agents may be enrolled, but must remain on stable doses of the agents from 7 days prior to Baseline Visit through to the follow-up visit at end of study.
    boolean
    C0282402 (UMLS CUI [1,1])
    C2349954 (UMLS CUI [1,2])
    C0282402 (UMLS CUI [2,1])
    C0579004 (UMLS CUI [2,2])
    C0282402 (UMLS CUI [3,1])
    C1707811 (UMLS CUI [3,2])
    C1827504 (UMLS CUI [4,1])
    C0008809 (UMLS CUI [4,2])
    C0008783 (UMLS CUI [4,3])
    C0085228 (UMLS CUI [4,4])
    C0282402 (UMLS CUI [4,5])
    C1827490 (UMLS CUI [5,1])
    C0543414 (UMLS CUI [5,2])
    C0028978 (UMLS CUI [5,3])
    12. Night workers or any others whose sleeping habits are incompatible with the study design, or who would be required to make significant changes to their bedtime during the course of the study.
    Item
    12. Night workers or any others whose sleeping habits are incompatible with the study design, or who would be required to make significant changes to their bedtime during the course of the study.
    boolean
    C0555008 (UMLS CUI [1])
    C0547101 (UMLS CUI [2,1])
    C4698019 (UMLS CUI [2,2])
    C0035171 (UMLS CUI [2,3])
    C0547101 (UMLS CUI [3,1])
    C4698019 (UMLS CUI [3,2])
    C0680104 (UMLS CUI [3,3])
    13. Subjects who have exhibited intolerance to ropinirole or any other dopamine agonist.
    Item
    13. Subjects who have exhibited intolerance to ropinirole or any other dopamine agonist.
    boolean
    C1744706 (UMLS CUI [1,1])
    C0244821 (UMLS CUI [1,2])
    C1744706 (UMLS CUI [2,1])
    C0178601 (UMLS CUI [2,2])
    14. Participation in any clinical drug or device trial in the one month prior to the Baseline Visit.
    Item
    14. Participation in any clinical drug or device trial in the one month prior to the Baseline Visit.
    boolean
    C2348568 (UMLS CUI [1])
    15. Subjects non-compliant with the visit schedule or other study procedures.
    Item
    15. Subjects who, in the opinion of the investigator, would be non-compliant with the visit schedule or other study procedures.
    boolean
    C1321605 (UMLS CUI [1,1])
    C2348563 (UMLS CUI [1,2])
    16. Women who have a positive pregnancy test or who are lactating.
    Item
    16. Women who have a positive pregnancy test or who are lactating.
    boolean
    C0032961 (UMLS CUI [1])
    C2828358 (UMLS CUI [2])
    17. Women of child-bearing potential who are not practicing a clinically accepted method of contraception.
    Item
    17. Women of child-bearing potential who are not practicing a clinically accepted method of contraception such as oral contraception, surgical sterilization, IUD, diaphragm in conjunction with spermicidal foam and condom on the male partner, or systemic contraception (e.g. Norplant).
    boolean
    C1960468 (UMLS CUI [1])
    C0700589 (UMLS CUI [2,1])
    C3176353 (UMLS CUI [2,2])
    C0029151 (UMLS CUI [3])
    C0015787 (UMLS CUI [4])
    C0021900 (UMLS CUI [5])
    C0042241 (UMLS CUI [6,1])
    C3843423 (UMLS CUI [6,2])
    C0009653 (UMLS CUI [6,3])
    C0700589 (UMLS CUI [7,1])
    C1515119 (UMLS CUI [7,2])
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