ID
35147
Description
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
Keywords
Versions (1)
- 2/19/19 2/19/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
February 19, 2019
DOI
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License
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
RLS Symptoms Diary, Screening/ Washout Phase;
- StudyEvent: ODM
Description
RLS Symptoms Diary - Screening/ Washout Phase
Alias
- UMLS CUI-1
- C0035258
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0220908
- UMLS CUI-4
- C1710661
Description
From 7 a.m. on
Data type
date
Alias
- UMLS CUI [1]
- C0808070
Description
to 6:59 a.m. on
Data type
date
Alias
- UMLS CUI [1]
- C0806020
Description
What was the first time your RLS symptoms began between the times above:
Data type
time
Alias
- UMLS CUI [1,1]
- C0035258
- UMLS CUI [1,2]
- C1457887
- UMLS CUI [1,3]
- C0700364
- UMLS CUI [1,4]
- C0205435
Description
Did you have RLS symptoms in this time frame?
Alias
- UMLS CUI-1
- C0035258
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0332168
Description
If Yes, continue below
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
If Yes, continue below
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
If Yes, continue below
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
Estimate of total number of hours of symptoms during time frame 1 e.g., enter 1 hour and 30 minutes as 1.30
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0449238
- UMLS CUI-3
- C0332168
Description
Cannot be greater than or equal to 10 hours.
Data type
float
Alias
- UMLS CUI [1]
- C0332168
Description
Cannot be greater than or equal to 3 hours.
Data type
float
Alias
- UMLS CUI [1]
- C0332168
Description
Cannot be greater than or equal to 11 hours.
Data type
float
Alias
- UMLS CUI [1]
- C0332168
Description
Location of symptoms during this time frame - Check all that apply:
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0450429
- UMLS CUI-3
- C0332168
Description
1. 7:00 a.m. to 4:59 p.m.
Data type
integer
Alias
- UMLS CUI [1]
- C0332168
Description
2. 5:00 p.m. to 7:59 p.m.
Data type
integer
Alias
- UMLS CUI [1]
- C0332168
Description
3. 8:00 p.m. to 6:59 a.m.
Data type
integer
Alias
- UMLS CUI [1]
- C0332168
Description
Maximum severity of symptoms during this time frame - Check one:
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0439793
- UMLS CUI-3
- C0806909
- UMLS CUI-4
- C0332168
Description
1. 7:00 a.m. to 4:59 p.m.
Data type
integer
Alias
- UMLS CUI [1]
- C0332168
Description
2. 5:00 p.m. to 7:59 p.m.
Data type
integer
Alias
- UMLS CUI [1]
- C0332168
Description
3. 8:00 p.m. to 6:59 a.m.
Data type
integer
Alias
- UMLS CUI [1]
- C0332168
Similar models
RLS Symptoms Diary, Screening/ Washout Phase;
- StudyEvent: ODM
C1457887 (UMLS CUI-2)
C0220908 (UMLS CUI-3)
C1710661 (UMLS CUI-4)
C1457887 (UMLS CUI [1,2])
C0700364 (UMLS CUI [1,3])
C0205435 (UMLS CUI [1,4])
C1457887 (UMLS CUI-2)
C0332168 (UMLS CUI-3)
C0449238 (UMLS CUI-2)
C0332168 (UMLS CUI-3)
C0450429 (UMLS CUI-2)
C0332168 (UMLS CUI-3)
C0439793 (UMLS CUI-2)
C0806909 (UMLS CUI-3)
C0332168 (UMLS CUI-4)