ID

22381

Beschrijving

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

Link

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

Trefwoorden

  1. 01-06-17 01-06-17 -
  2. 12-06-17 12-06-17 -
Geüploaded op

1 juni 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862 - Visit 8 (Week 15) PRN Subject Diary

Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

General Information
Beschrijving

General Information

Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Date of Beginning
Beschrijving

Date of Beginning

Datatype

date

Date of End
Beschrijving

Date of End

Datatype

date

RLS episode
Beschrijving

RLS episode

Date of RLS Episode
Beschrijving

Date of RLS Episode

Datatype

date

Treatment of RLS Episode
Beschrijving

Treatment of RLS Episode

Datatype

text

Similar models

Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
General Information
Subject Identifier
Item
Subject Identifier
text
Date of Beginning
Item
Date of Beginning
date
Date of End
Item
Date of End
date
Item Group
RLS episode
Date of RLS Episode
Item
Date of RLS Episode
date
Item
Treatment of RLS Episode
text
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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