ID

24540

Description

Study part: Investigational Product. 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. 8/5/17 8/5/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 5, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Investigational Product Ropinirole Restless Legs Syndrom NCT00355641

English

Investigational Product

1 forms  
INVESTIGATIONAL PRODUCT
Description

INVESTIGATIONAL PRODUCT

Alias
UMLS CUI-1
C0304229
Date and time of in-clinic dose
Description

date and time dose

Data type

datetime

Alias
UMLS CUI [1]
C1986447
Dosing end date
Description

end date dose

Data type

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0178602
Dose
Description

Dose

Data type

float

Alias
UMLS CUI [1]
C3174092
Unit
Description

Unit

Data type

text

Alias
UMLS CUI [1]
C1519795
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Similar models

Investigational Product

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
INVESTIGATIONAL PRODUCT
C0304229 (UMLS CUI-1)
date and time dose
Item
Date and time of in-clinic dose
datetime
C1986447 (UMLS CUI [1])
end date dose
Item
Dosing end date
date
C0806020 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Dose
Item
Dose
float
C3174092 (UMLS CUI [1])
Unit
Item
Unit
text
C1519795 (UMLS CUI [1])
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