ID
35147
Descripción
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
Palabras clave
Versiones (1)
- 19/2/19 19/2/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
19 de febrero de 2019
DOI
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Licencia
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
Descripción
RLS Symptoms Diary - Screening/ Washout Phase
Alias
- UMLS CUI-1
- C0035258
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0220908
- UMLS CUI-4
- C1710661
Descripción
From 7 a.m. on
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0808070
Descripción
to 6:59 a.m. on
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0806020
Descripción
What was the first time your RLS symptoms began between the times above:
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0035258
- UMLS CUI [1,2]
- C1457887
- UMLS CUI [1,3]
- C0700364
- UMLS CUI [1,4]
- C0205435
Descripción
Did you have RLS symptoms in this time frame?
Alias
- UMLS CUI-1
- C0035258
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0332168
Descripción
If Yes, continue below
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0332168
Descripción
If Yes, continue below
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0332168
Descripción
If Yes, continue below
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0332168
Descripción
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
Descripción
Cannot be greater than or equal to 10 hours.
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0332168
Descripción
Cannot be greater than or equal to 3 hours.
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0332168
Descripción
Cannot be greater than or equal to 11 hours.
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0332168
Descripción
Location of symptoms during this time frame - Check all that apply:
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0450429
- UMLS CUI-3
- C0332168
Descripción
1. 7:00 a.m. to 4:59 p.m.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0332168
Descripción
2. 5:00 p.m. to 7:59 p.m.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0332168
Descripción
3. 8:00 p.m. to 6:59 a.m.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0332168
Descripción
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
Descripción
1. 7:00 a.m. to 4:59 p.m.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0332168
Descripción
2. 5:00 p.m. to 7:59 p.m.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0332168
Descripción
3. 8:00 p.m. to 6:59 a.m.
Tipo de datos
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)