ID

22797

Description

Study ID: 100310 Clinical Study ID: RRL100310 Study Title: A 12-week, double-blind, placebo-controlled, parallel group study to assess the efficacy and safety of intermittent dosing of ropinirole in patients with Restless Legs Syndrome (RLS) Part 1: Visit 8 (Week 15) PRN Subject Diary Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00225862 Sponsor: GlaxoSmithKline Collaborators: N/A 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 More details on: https://clinicaltrials.gov/ct2/show/NCT00225862

Lien

https://clinicaltrials.gov/ct2/show/NCT00225862

Mots-clés

Versions (2)
  1. 01/06/2017 01/06/2017 -
  2. 12/06/2017 12/06/2017 -
Téléchargé le

12 juin 2017

DOI

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Licence

Creative Commons BY-NC 3.0
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Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

Anglais

Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

1 Formulaires  
General Information
Description

General Information

Alias
UMLS CUI-1
C1508263
UMLS CUI-2
C1955348
UMLS CUI-3
C0035258
Subject Identifier
Description

Subject Identifier

Type de données

text

Alias
UMLS CUI [1]
C2348585
Date of Beginning
Description

Date of Beginning

Type de données

date

Alias
UMLS CUI [1]
C0808070
Date of End
Description

Date of End

Type de données

date

Alias
UMLS CUI [1]
C0806020
RLS episode
Description

RLS episode

Alias
UMLS CUI-1
C0035258
UMLS CUI-2
C0332189
Date of RLS Episode
Description

Date of RLS Episode

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0035258
UMLS CUI [1,3]
C0332189
Treatment of RLS Episode
Description

Treatment of RLS Episode

Type de données

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0035258
UMLS CUI [1,3]
C0332189
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Similar models

Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
General Information
C1508263 (UMLS CUI-1)
C1955348 (UMLS CUI-2)
C0035258 (UMLS CUI-3)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Date of Beginning
Item
Date of Beginning
date
C0808070 (UMLS CUI [1])
Date of End
Item
Date of End
date
C0806020 (UMLS CUI [1])
Item Group
RLS episode
C0035258 (UMLS CUI-1)
C0332189 (UMLS CUI-2)
Date of RLS Episode
Item
Date of RLS Episode
date
C0011008 (UMLS CUI [1,1])
C0035258 (UMLS CUI [1,2])
C0332189 (UMLS CUI [1,3])
Item
Treatment of RLS Episode
text
C0087111 (UMLS CUI [1,1])
C0035258 (UMLS CUI [1,2])
C0332189 (UMLS CUI [1,3])
Treatment of RLS Episode
Code List
Treatment of RLS Episode
CL Item
RLS episode has been treated.  (1)
CL Item
RLS episode has not been treated. (2)
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