ID
35147
Beschreibung
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
Stichworte
Versionen (1)
- 19.02.19 19.02.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
19. Februar 2019
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome NCT00197080
RLS Symptoms Diary, Screening/ Washout Phase;
- StudyEvent: ODM
Beschreibung
RLS Symptoms Diary - Screening/ Washout Phase
Alias
- UMLS CUI-1
- C0035258
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0220908
- UMLS CUI-4
- C1710661
Beschreibung
From 7 a.m. on
Datentyp
date
Alias
- UMLS CUI [1]
- C0808070
Beschreibung
to 6:59 a.m. on
Datentyp
date
Alias
- UMLS CUI [1]
- C0806020
Beschreibung
What was the first time your RLS symptoms began between the times above:
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0035258
- UMLS CUI [1,2]
- C1457887
- UMLS CUI [1,3]
- C0700364
- UMLS CUI [1,4]
- C0205435
Beschreibung
Did you have RLS symptoms in this time frame?
Alias
- UMLS CUI-1
- C0035258
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0332168
Beschreibung
If Yes, continue below
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
If Yes, continue below
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
If Yes, continue below
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
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
Beschreibung
Cannot be greater than or equal to 10 hours.
Datentyp
float
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
Cannot be greater than or equal to 3 hours.
Datentyp
float
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
Cannot be greater than or equal to 11 hours.
Datentyp
float
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
Location of symptoms during this time frame - Check all that apply:
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0450429
- UMLS CUI-3
- C0332168
Beschreibung
1. 7:00 a.m. to 4:59 p.m.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
2. 5:00 p.m. to 7:59 p.m.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
3. 8:00 p.m. to 6:59 a.m.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
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
Beschreibung
1. 7:00 a.m. to 4:59 p.m.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
2. 5:00 p.m. to 7:59 p.m.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0332168
Beschreibung
3. 8:00 p.m. to 6:59 a.m.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0332168
Ähnliche Modelle
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)