ID
24693
Description
Study part: RLS Symptoms on the first day of the patient RLS Symptoms diary prior to the Baseline Visit. 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)
- 8/13/17 8/13/17 -
Copyright Holder
GlaxoSmithKline
Uploaded on
August 13, 2017
DOI
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License
Creative Commons BY-NC 3.0
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RLS Symptoms on the first day of the patient RLS Symptoms diary prior to the Baseline Visit Ropinirole Restless Legs Syndrom NCT00355641
RLS Symptoms on the first day of the patient RLS Symptoms diary prior to the Baseline Visit
Description
RLS Symptoms on the first day of the patient
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0035258
Description
From 07:00 on the morning to 06:59 of the next morning.
Data type
date
Alias
- UMLS CUI [1]
- C0011008
Description
Symptoms RLS
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0035258
Description
time
Data type
time
Alias
- UMLS CUI [1]
- C0040223
Description
time fall sleep
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C3830397
Description
time wake up
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C1170730
Description
site
Data type
integer
Alias
- UMLS CUI [1]
- C1515974
Description
time frame
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Data type
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Data type
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Data type
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Data type
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Data type
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Data type
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Data type
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Data type
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Data type
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Data type
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Description
time frame
Data type
boolean
Alias
- UMLS CUI [1]
- C0332168
Description
symptom severity
Data type
text
Alias
- UMLS CUI [1]
- C1319166
Description
symptom Beginning
Data type
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0439659
Similar models
RLS Symptoms on the first day of the patient RLS Symptoms diary prior to the Baseline Visit
C0035258 (UMLS CUI-2)
C0035258 (UMLS CUI [1,2])
C3830397 (UMLS CUI [1,2])
C1170730 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])