ID

24584

Description

Study part: RLS Concomitant Medications - Ropinirole (CM RLS (2)). 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. 8/7/17 8/7/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 7, 2017

DOI

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License

Creative Commons BY-NC 3.0
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RLS Concomitant Medications - Ropinirole (CM RLS (2)) Ropinirole Restless Legs Syndrom NCT00355641

English

RLS Concomitant Medications - Ropinirole (CM RLS (2))

1 forms  
RLS CONCOMITANT MEDICATIONS - ROPINIROLE (CM RLS (2))
Description

RLS CONCOMITANT MEDICATIONS - ROPINIROLE (CM RLS (2))

Alias
UMLS CUI-1
C2347852
1. Ropinirole. Was drug ever used?
Description

Ropinirole

Data type

boolean

Alias
UMLS CUI [1]
C0244821
Start Date:
Description

Start Date

Data type

date

Alias
UMLS CUI [1]
C0808070
End Date:
Description

End Date

Data type

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Description

respond to treatment

Data type

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Description

tolerate treatment

Data type

boolean

Alias
UMLS CUI [1]
C0013220
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Similar models

RLS Concomitant Medications - Ropinirole (CM RLS (2))

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
RLS CONCOMITANT MEDICATIONS - ROPINIROLE (CM RLS (2))
C2347852 (UMLS CUI-1)
Ropinirole
Item
1. Ropinirole. Was drug ever used?
boolean
C0244821 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
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