ID

24663

Description

Study part: Assessment Of Rebound (RBND). 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

  1. 8/12/17 8/12/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 12, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Assessment Of Rebound (RBND) Ropinirole Restless Legs Syndrom NCT00355641

Assessment Of Rebound (RBND)

ASSESSMENT OF REBOUND (RBND)
Description

ASSESSMENT OF REBOUND (RBND)

Alias
UMLS CUI-1
C0220825
1. RLS rebound experienced at end of dose?
Description

End of dose rebound, defined as a re-emergence of RLS symptoms in the early morning the day after taking the dose of RLS medication.

Data type

boolean

Alias
UMLS CUI [1,1]
C0549262
UMLS CUI [1,2]
C0035258
2. Assessor
Description

Assessor

Data type

text

Alias
UMLS CUI [1]
C2646699

Similar models

Assessment Of Rebound (RBND)

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
ASSESSMENT OF REBOUND (RBND)
C0220825 (UMLS CUI-1)
rebound RLS
Item
1. RLS rebound experienced at end of dose?
boolean
C0549262 (UMLS CUI [1,1])
C0035258 (UMLS CUI [1,2])
Item
2. Assessor
text
C2646699 (UMLS CUI [1])
Code List
2. Assessor
CL Item
Investigator (Investigator)
CL Item
Health care professional or nurse (Health care professional or nurse)

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