ID

22576

Beskrivning

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 23: Visit 4 (Week 7) 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

Länk

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

Nyckelord

  1. 2017-06-08 2017-06-08 -
  2. 2017-06-12 2017-06-12 -
Uppladdad den

8 juni 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862 - Part 23: Visit 4 (Week 7) PRN Subject Diary

Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862 - Part 23: Visit 4 (Week 7) PRN Subject Diary

General Information
Beskrivning

General Information

Subject Identifier
Beskrivning

Subject Identifier

Datatyp

text

Date of Beginning
Beskrivning

Date of Beginning

Datatyp

date

Date of End
Beskrivning

Date of End

Datatyp

date

RLS episode
Beskrivning

RLS episode

Date of RLS Episode
Beskrivning

Date of RLS Episode

Datatyp

date

Treatment of RLS Episode
Beskrivning

Treatment of RLS Episode

Datatyp

text

Similar models

Intermittent Ropinirole in Restless Legs Syndrome (RLS) NCT00225862 - Part 23: Visit 4 (Week 7) PRN Subject Diary

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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