ID
24701
Description
Study part: RLS Symptoms on the first day of the patient RLS Symptoms Diary prior to the Week 36 Visit . A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Clinicaltrials.gov Identifier: NCT00355641. 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. Study ID: 101468/206. Clinical Study ID: 101468/206.
Mots-clés
Versions (1)
- 13/08/2017 13/08/2017 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
13 août 2017
DOI
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Licence
Creative Commons BY-NC 3.0
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RLS Symptoms on the first day of the patient RLS Symptoms Diary prior to the Week 36 Visit Ropinirole Restless Legs Syndrom NCT00355641
RLS Symptoms on the first day of the patient RLS Symptoms Diary prior to the Week 36 Visit
Description
RLS Symptoms on the first day of the patient
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0035258
Description
From 07:00 on the morning to 06:59 of the next morning.
Type de données
date
Alias
- UMLS CUI [1]
- C0011008
Description
medication
Type de données
boolean
Alias
- UMLS CUI [1]
- C0013227
Description
time medication intake
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C1512806
Description
Symptoms RLS
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0035258
Description
time
Type de données
time
Alias
- UMLS CUI [1]
- C0040223
Description
time fall sleep
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C3830397
Description
time wake up
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C1170730
Description
site
Type de données
integer
Alias
- UMLS CUI [1]
- C1515974
Description
time frame
Type de données
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Type de données
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Type de données
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Type de données
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Type de données
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Type de données
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Type de données
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Type de données
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Type de données
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Type de données
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Type de données
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Type de données
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Similar models
RLS Symptoms on the first day of the patient RLS Symptoms Diary prior to the Week 36 Visit
C0035258 (UMLS CUI-2)
C0013227 (UMLS CUI [1,2])
C1512806 (UMLS CUI [1,3])
C0035258 (UMLS CUI [1,2])
C3830397 (UMLS CUI [1,2])
C1170730 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])