ID

24521

Description

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.

Keywords

Versions (1)
  1. 8/4/17 8/4/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 4, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

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

English

Previous Clinical Trial Participation

1 forms  
PREVIOUS CLINICAL TRIAL PARTICIPATION
Description

PREVIOUS CLINICAL TRIAL PARTICIPATION

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

Study Subject Participation Status

Data type

boolean

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

Study ID

Data type

text

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

Centre Number

Data type

integer

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

Subject number

Data type

text

Alias
UMLS CUI [1]
C2348585
Back to the top of the page

Similar models

Previous Clinical Trial Participation

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial