ID

24521

Beschrijving

Study part: Previous Clinical Trial Participation.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.

Trefwoorden

  1. 04-08-17 04-08-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

4 augustus 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Previous Clinical Trial Participation(PRVTRIAL) Ropinirole Restless Legs Syndrom NCT00355641

Previous Clinical Trial Participation

PREVIOUS CLINICAL TRIAL PARTICIPATION
Beschrijving

PREVIOUS CLINICAL TRIAL PARTICIPATION

Alias
UMLS CUI-1
C2348568
1. Did the subject participate in any of the following studies: 101468/205 or ROX104805?
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
If yes, previous Study identifier
Beschrijving

Study ID

Datatype

text

Alias
UMLS CUI [1]
C2826693
If yes, previous Centre number
Beschrijving

Centre Number

Datatype

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
If yes, previous Subject number
Beschrijving

Subject number

Datatype

text

Alias
UMLS CUI [1]
C2348585

Similar models

Previous Clinical Trial Participation

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
PREVIOUS CLINICAL TRIAL PARTICIPATION
C2348568 (UMLS CUI-1)
Study Subject Participation Status
Item
1. Did the subject participate in any of the following studies: 101468/205 or ROX104805?
boolean
C2348568 (UMLS CUI [1])
Study ID
Item
If yes, previous Study identifier
text
C2826693 (UMLS CUI [1])
Centre Number
Item
If yes, previous Centre number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Subject number
Item
If yes, previous Subject number
text
C2348585 (UMLS CUI [1])

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