ID
40758
Beschrijving
Study ID: 101468/218 Clinical Study ID: SKF-101468/218 Study Title:A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome
Trefwoorden
Versies (4)
- 27-04-20 27-04-20 -
- 04-05-20 04-05-20 -
- 08-05-20 08-05-20 -
- 08-05-20 08-05-20 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
8 mei 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218
Predose Checklist; Las Visit Checklist
- StudyEvent: ODM
Beschrijving
Predose Checklist (Day 1)
Alias
- UMLS CUI-1
- C0439565
- UMLS CUI-2
- C1707357
Beschrijving
1. Has the patient washed out from their previous RLS medication for the appropiate length of time? (DAY 1)
Datatype
boolean
Alias
- UMLS CUI [1]
- C1710661
- UMLS CUI [2,1]
- C0013216
- UMLS CUI [2,2]
- C0035258
- UMLS CUI [2,3]
- C0205156
- UMLS CUI [3]
- C0449238
Beschrijving
2. Has the patient refrained from consuming alcohol for 24 hours prior to the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C1517741
Beschrijving
3. Has the patient limited their daily alcohol consumption to no more than 3 units for men and 2 units for women? (1 unit is equivalent to 1 beer, one measure of sprits or 1 small glass of wine.)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2]
- C0560579
- UMLS CUI [3]
- C0559430
- UMLS CUI [4]
- C0043188
Beschrijving
4. Has the patient refrained from strenuous exercise (outside of normal routine) from 48 hours before the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1514989
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2,1]
- C0008952
- UMLS CUI [2,2]
- C0332152
Beschrijving
5. Has the patient maintained their normal smoking practice?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519386
Beschrijving
6. Has the patient refrained from fluctuating dose of oestrogen ie. in hormone replacement therapy (HRT) or oral contraceptives?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0279494
- UMLS CUI [1,2]
- C0678766
- UMLS CUI [1,3]
- C0231241
- UMLS CUI [1,4]
- C0282402
- UMLS CUI [2]
- C0029151
Beschrijving
7. Taking medication (activity); Other; Restricted | OTC - Over The Counter | Medicinal Herbs | Clinic Visits; Before | Interferes with; Procedure (set of actions); Clinical Research
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0443288
- UMLS CUI [2]
- C2709201
- UMLS CUI [3]
- C0025125
- UMLS CUI [4,1]
- C0008952
- UMLS CUI [4,2]
- C0332152
- UMLS CUI [5,1]
- C0521102
- UMLS CUI [5,2]
- C2700391
- UMLS CUI [5,3]
- C0008972
Beschrijving
8. Has the patient washed out from any previous prohibited medication for the appropriate length of time?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710661
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0683610
- UMLS CUI [1,4]
- C0205156
- UMLS CUI [2]
- C0449238
Beschrijving
9. For the concomitant medications which are CYP1A2 inducers, substrates or inhibitors, has the patient kept the dose constant
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C1827490
- UMLS CUI [2,1]
- C0207509
- UMLS CUI [2,2]
- C0178623
- UMLS CUI [3]
- C1827504
- UMLS CUI [4,1]
- C0178602
- UMLS CUI [4,2]
- C1948059
- UMLS CUI [5]
- C0282402
Beschrijving
10. Has the patient completed 2 consecutive nights of baseline actigraphy and ambulatory sleep EEG recordings at home?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1442488
- UMLS CUI [2,1]
- C1171301
- UMLS CUI [2,2]
- C0013819
- UMLS CUI [2,3]
- C0037313
- UMLS CUI [3,1]
- C0013819
- UMLS CUI [3,2]
- C0037313
- UMLS CUI [3,3]
- C0439841
Beschrijving
11. Has the patient completed the St Mary’s Sleep Questionnaire at home?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0034394
- UMLS CUI [1,2]
- C0037313
Beschrijving
Predose Checklist (Day 3; Extra Clinic Visit 1- 3)
Alias
- UMLS CUI-1
- C0439565
- UMLS CUI-2
- C1707357
Beschrijving
1. Has the patient refrained from consuming alcohol for 24 hours prior to the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C1517741
Beschrijving
2. Has the patient limited their daily alcohol consumption to no more than 3 units for men and 2 units for women?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2]
- C0560579
- UMLS CUI [3]
- C0559430
- UMLS CUI [4]
- C0043188
Beschrijving
3. Has the patient refrained from strenuous exercise (outside of normal routine) from 48 hours before the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1514989
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2,1]
- C0008952
- UMLS CUI [2,2]
- C0332152
Beschrijving
4. Has the patient maintained their normal smoking practice?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519386
Beschrijving
5. Has the patient refrained from fluctuating dose of oestrogen ie. in hormone replacement therapy (HRT) or oral contraceptives?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0279494
- UMLS CUI [1,2]
- C0678766
- UMLS CUI [1,3]
- C0231241
- UMLS CUI [1,4]
- C0282402
- UMLS CUI [2]
- C0029151
Beschrijving
6. Taking medication (activity); Other; Restricted | OTC - Over The Counter | Medicinal Herbs | Clinic Visits; Before | Interferes with; Procedure (set of actions); Clinical Research
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0443288
- UMLS CUI [2]
- C2709201
- UMLS CUI [3]
- C0025125
- UMLS CUI [4,1]
- C0008952
- UMLS CUI [4,2]
- C0332152
- UMLS CUI [5,1]
- C0521102
- UMLS CUI [5,2]
- C2700391
- UMLS CUI [5,3]
- C0008972
Beschrijving
7. For the concomitant medications which are CYP1A2 inducers, substrates or inhibitors, has the patient kept the dose constant? (this includes women taking hormone replacement therapy (HRT) or oestrogen containing medications)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C1827490
- UMLS CUI [2,1]
- C0207509
- UMLS CUI [2,2]
- C0178623
- UMLS CUI [3]
- C1827504
- UMLS CUI [4,1]
- C0178602
- UMLS CUI [4,2]
- C1948059
- UMLS CUI [5]
- C0282402
Beschrijving
Predose Checklist (Day 15, Day 22, Day 29, Day 36, Day 43)
Alias
- UMLS CUI-1
- C0439565
- UMLS CUI-2
- C1707357
Beschrijving
1. Has the patient refrained from consuming alcohol for 24 hours prior to the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C1517741
Beschrijving
2. Has the patient limited their daily alcohol consumption to no more than 3 units for men and 2 units for women?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2]
- C0560579
- UMLS CUI [3]
- C0559430
- UMLS CUI [4]
- C0043188
Beschrijving
3. Has the patient refrained from strenuous exercise (outside of normal routine) from 48 hours before the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1514989
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2,1]
- C0008952
- UMLS CUI [2,2]
- C0332152
Beschrijving
4. Has the patient maintained their normal smoking practice?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519386
Beschrijving
5. Has the patient refrained from fluctuating dose of oestrogen ie. in hormone replacement therapy (HRT) or oral contraceptives?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0279494
- UMLS CUI [1,2]
- C0678766
- UMLS CUI [1,3]
- C0231241
- UMLS CUI [1,4]
- C0282402
- UMLS CUI [2]
- C0029151
Beschrijving
6. Taking medication (activity); Other; Restricted | OTC - Over The Counter | Medicinal Herbs | Clinic Visits; Before | Interferes with; Procedure (set of actions); Clinical Research
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0443288
- UMLS CUI [2]
- C2709201
- UMLS CUI [3]
- C0025125
- UMLS CUI [4,1]
- C0008952
- UMLS CUI [4,2]
- C0332152
- UMLS CUI [5,1]
- C0521102
- UMLS CUI [5,2]
- C2700391
- UMLS CUI [5,3]
- C0008972
Beschrijving
7. For the concomitant medications which are CYP1A2 inducers, substrates or inhibitors, has the patient kept the dose constant? (this includes women taking hormone replacement therapy (HRT) or oestrogen containing medications)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C1827490
- UMLS CUI [2,1]
- C0207509
- UMLS CUI [2,2]
- C0178623
- UMLS CUI [3]
- C1827504
- UMLS CUI [4,1]
- C0178602
- UMLS CUI [4,2]
- C1948059
- UMLS CUI [5]
- C0282402
Beschrijving
8. Has the patient completed actigraphy and EEG recordings on 2 consecutive nights and completed the St Mary’s Sleep Questionnaire
Datatype
boolean
Alias
- UMLS CUI [1]
- C1171301
- UMLS CUI [2]
- C0013819
- UMLS CUI [3,1]
- C0034394
- UMLS CUI [3,2]
- C0037313
Beschrijving
Last Visit Checklist
Alias
- UMLS CUI-1
- C1707357
- UMLS CUI-2
- C0545082
- UMLS CUI-3
- C1517741
Beschrijving
1. Has the patient refrained from consuming alcohol for 24 hours prior to the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C1517741
Beschrijving
2. Has the patient limited their daily alcohol consumption to no more than 3 units for men and 2 units for women?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2]
- C0560579
- UMLS CUI [3]
- C0559430
- UMLS CUI [4]
- C0043188
Beschrijving
3. Has the patient refrained from strenuous exercise (outside of normal routine) from 48 hours before the clinic visit?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1514989
- UMLS CUI [1,2]
- C0443288
- UMLS CUI [2,1]
- C0008952
- UMLS CUI [2,2]
- C0332152
Beschrijving
4. Has the patient maintained their normal smoking practice?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519386
Beschrijving
5. Has the patient refrained from fluctuating dose of oestrogen ie. in hormone replacement therapy (HRT) or oral contraceptives?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0279494
- UMLS CUI [1,2]
- C0678766
- UMLS CUI [1,3]
- C0231241
- UMLS CUI [1,4]
- C0282402
- UMLS CUI [2]
- C0029151
Beschrijving
6. Taking medication (activity); Other; Restricted | OTC - Over The Counter | Medicinal Herbs | Clinic Visits; Before | Interferes with; Procedure (set of actions); Clinical Research
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0443288
- UMLS CUI [2]
- C2709201
- UMLS CUI [3]
- C0025125
- UMLS CUI [4,1]
- C0008952
- UMLS CUI [4,2]
- C0332152
- UMLS CUI [5,1]
- C0521102
- UMLS CUI [5,2]
- C2700391
- UMLS CUI [5,3]
- C0008972
Beschrijving
7. For the concomitant medications which are CYP1A2 inducers, substrates or inhibitors, has the patient kept the dose constant? (this includes women taking hormone replacement therapy (HRT) or oestrogen containing medications)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C1827490
- UMLS CUI [2,1]
- C0207509
- UMLS CUI [2,2]
- C0178623
- UMLS CUI [3]
- C1827504
- UMLS CUI [4,1]
- C0178602
- UMLS CUI [4,2]
- C1948059
- UMLS CUI [5]
- C0282402
Beschrijving
8. Has the patient completed actigraphy and EEG recordings on 2 consecutive nights and completed the St Mary’s Sleep Questionnaire
Datatype
boolean
Alias
- UMLS CUI [1]
- C1171301
- UMLS CUI [2]
- C0013819
- UMLS CUI [3,1]
- C0034394
- UMLS CUI [3,2]
- C0037313
Similar models
Predose Checklist; Las Visit Checklist
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C1707357 (UMLS CUI-2)
C0013216 (UMLS CUI [2,1])
C0035258 (UMLS CUI [2,2])
C0205156 (UMLS CUI [2,3])
C0449238 (UMLS CUI [3])
C1517741 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,2])
C0560579 (UMLS CUI [2])
C0559430 (UMLS CUI [3])
C0043188 (UMLS CUI [4])
C0443288 (UMLS CUI [1,2])
C0008952 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C0678766 (UMLS CUI [1,2])
C0231241 (UMLS CUI [1,3])
C0282402 (UMLS CUI [1,4])
C0029151 (UMLS CUI [2])
C0205394 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,3])
C2709201 (UMLS CUI [2])
C0025125 (UMLS CUI [3])
C0008952 (UMLS CUI [4,1])
C0332152 (UMLS CUI [4,2])
C0521102 (UMLS CUI [5,1])
C2700391 (UMLS CUI [5,2])
C0008972 (UMLS CUI [5,3])
C0013227 (UMLS CUI [1,2])
C0683610 (UMLS CUI [1,3])
C0205156 (UMLS CUI [1,4])
C0449238 (UMLS CUI [2])
C1827490 (UMLS CUI [1,2])
C0207509 (UMLS CUI [2,1])
C0178623 (UMLS CUI [2,2])
C1827504 (UMLS CUI [3])
C0178602 (UMLS CUI [4,1])
C1948059 (UMLS CUI [4,2])
C0282402 (UMLS CUI [5])
C1171301 (UMLS CUI [2,1])
C0013819 (UMLS CUI [2,2])
C0037313 (UMLS CUI [2,3])
C0013819 (UMLS CUI [3,1])
C0037313 (UMLS CUI [3,2])
C0439841 (UMLS CUI [3,3])
C0037313 (UMLS CUI [1,2])
C1707357 (UMLS CUI-2)
C1517741 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,2])
C0560579 (UMLS CUI [2])
C0559430 (UMLS CUI [3])
C0043188 (UMLS CUI [4])
C0443288 (UMLS CUI [1,2])
C0008952 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C0678766 (UMLS CUI [1,2])
C0231241 (UMLS CUI [1,3])
C0282402 (UMLS CUI [1,4])
C0029151 (UMLS CUI [2])
C0205394 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,3])
C2709201 (UMLS CUI [2])
C0025125 (UMLS CUI [3])
C0008952 (UMLS CUI [4,1])
C0332152 (UMLS CUI [4,2])
C0521102 (UMLS CUI [5,1])
C2700391 (UMLS CUI [5,2])
C0008972 (UMLS CUI [5,3])
C1827490 (UMLS CUI [1,2])
C0207509 (UMLS CUI [2,1])
C0178623 (UMLS CUI [2,2])
C1827504 (UMLS CUI [3])
C0178602 (UMLS CUI [4,1])
C1948059 (UMLS CUI [4,2])
C0282402 (UMLS CUI [5])
C1707357 (UMLS CUI-2)
C1517741 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,2])
C0560579 (UMLS CUI [2])
C0559430 (UMLS CUI [3])
C0043188 (UMLS CUI [4])
C0443288 (UMLS CUI [1,2])
C0008952 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C0678766 (UMLS CUI [1,2])
C0231241 (UMLS CUI [1,3])
C0282402 (UMLS CUI [1,4])
C0029151 (UMLS CUI [2])
C0205394 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,3])
C2709201 (UMLS CUI [2])
C0025125 (UMLS CUI [3])
C0008952 (UMLS CUI [4,1])
C0332152 (UMLS CUI [4,2])
C0521102 (UMLS CUI [5,1])
C2700391 (UMLS CUI [5,2])
C0008972 (UMLS CUI [5,3])
C1827490 (UMLS CUI [1,2])
C0207509 (UMLS CUI [2,1])
C0178623 (UMLS CUI [2,2])
C1827504 (UMLS CUI [3])
C0178602 (UMLS CUI [4,1])
C1948059 (UMLS CUI [4,2])
C0282402 (UMLS CUI [5])
C0013819 (UMLS CUI [2])
C0034394 (UMLS CUI [3,1])
C0037313 (UMLS CUI [3,2])
C0545082 (UMLS CUI-2)
C1517741 (UMLS CUI-3)
C1517741 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,2])
C0560579 (UMLS CUI [2])
C0559430 (UMLS CUI [3])
C0043188 (UMLS CUI [4])
C0443288 (UMLS CUI [1,2])
C0008952 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C0678766 (UMLS CUI [1,2])
C0231241 (UMLS CUI [1,3])
C0282402 (UMLS CUI [1,4])
C0029151 (UMLS CUI [2])
C0205394 (UMLS CUI [1,2])
C0443288 (UMLS CUI [1,3])
C2709201 (UMLS CUI [2])
C0025125 (UMLS CUI [3])
C0008952 (UMLS CUI [4,1])
C0332152 (UMLS CUI [4,2])
C0521102 (UMLS CUI [5,1])
C2700391 (UMLS CUI [5,2])
C0008972 (UMLS CUI [5,3])
C1827490 (UMLS CUI [1,2])
C0207509 (UMLS CUI [2,1])
C0178623 (UMLS CUI [2,2])
C1827504 (UMLS CUI [3])
C0178602 (UMLS CUI [4,1])
C1948059 (UMLS CUI [4,2])
C0282402 (UMLS CUI [5])
C0013819 (UMLS CUI [2])
C0034394 (UMLS CUI [3,1])
C0037313 (UMLS CUI [3,2])
Geen commentaren