ID
29008
Description
Study ID: 101468/249 Clinical Study ID: 101468/249 Study Title: A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363857 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: N/A 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; Restless Legs Syndrome (RLS)
Mots-clés
Versions (1)
- 20/02/2018 20/02/2018 -
Détendeur de droits
GlaxoSmithKline (GSK)
Téléchargé le
20 février 2018
DOI
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Licence
Creative Commons BY-NC 3.0
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Clinical Study, Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS), Study ID: 101468/249, NCT00363857
RLS Demographics and Examination Procedure
- StudyEvent: ODM
Description
Vital signs
Alias
- UMLS CUI-1
- C0518766
Description
Height
Type de données
integer
Unités de mesure
- cm / in
Alias
- UMLS CUI [1]
- C0005890
Description
Weight
Type de données
integer
Unités de mesure
- kg / lbs
Alias
- UMLS CUI [1]
- C0005910
Description
Pulse
Type de données
integer
Unités de mesure
- beats/min
Alias
- UMLS CUI [1]
- C0232117
Description
Sitting Blood Pressure
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0580946
Description
Orthostatic vital signs
Alias
- UMLS CUI-1
- C0518766
Description
Screening
Type de données
integer
Alias
- UMLS CUI [1]
- C0220908
Description
Time
Type de données
time
Alias
- UMLS CUI [1]
- C0040223
Description
Blood Pressure
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0005823
Description
Pulse
Type de données
integer
Unités de mesure
- beats/min
Alias
- UMLS CUI [1]
- C0232117
Description
Electrocardiogram
Alias
- UMLS CUI-1
- C0430456
Description
Date of ECG
Type de données
date
Alias
- UMLS CUI [1]
- C2826640
Description
If ’Yes’, please record details on the Significant Medical/Surgical History and Physical Examination or Baseline Signs and Symptoms/SAE pages and repeat prior to baseline.
Type de données
integer
Alias
- UMLS CUI [1]
- C0522055
Description
Laboratory evaluation
Alias
- UMLS CUI-1
- C0022885
Description
Read the instructions on the Quest Diagnostics shipment document and dispatch the samples for analysis accordingly.
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
Description
If ’Yes’, please record details on the Significant Medical/Surgical History and Physical Examination or Baseline Signs and Symptoms/SAE pages and repeat prior to baseline.
Type de données
text
Alias
- UMLS CUI [1]
- C1853129
Description
Pregnancy Dipstick
Alias
- UMLS CUI-1
- C0430056
Description
If ’Yes’, please perform a pregnancy dipstick test and record result below.
Type de données
text
Alias
- UMLS CUI [1]
- C1960468
Description
If ’Positive’, please record details on the Significant Medical/Surgical History and Physical Examination and exclude the patient.
Type de données
text
Alias
- UMLS CUI [1]
- C0430056
Similar models
RLS Demographics and Examination Procedure
- StudyEvent: ODM
C0011008 (UMLS CUI [1,2])