ID
25640
Beschrijving
Study part: Serious Adverse Events (SAE). A Single Blind, Parallel Group, Up-titration, Phase 1 Study in Healthy Volunteers to Determine a Starting Dose and Select an Up-titration Regimen for a new Formulation of Ropinirole. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Phase: phase 1. 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: 101468/201. Clinical Study ID: 101468/201
Trefwoorden
Versies (2)
- 08-09-17 08-09-17 -
- 10-05-19 10-05-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
8 september 2017
DOI
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Licentie
Creative Commons BY-NC 3.0
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Serious Adverse Events (SAE) Ropinirole Restless Legs Syndrome 101468/201
Serious Adverse Experiences (SAE)
- StudyEvent: ODM
Beschrijving
RELEVANT LABORATORY DATA
Alias
- UMLS CUI-1
- C0022877
Beschrijving
Test
Datatype
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C0332307
Beschrijving
Date
Datatype
text
Alias
- UMLS CUI [1]
- C0011008
Beschrijving
Value
Datatype
text
Alias
- UMLS CUI [1]
- C1522609
Beschrijving
Units
Datatype
text
Alias
- UMLS CUI [1]
- C1519795
Beschrijving
Normal Range
Datatype
text
Alias
- UMLS CUI [1]
- C0086715
Beschrijving
Remarks
Datatype
text
Alias
- UMLS CUI [1]
- C0947611
Beschrijving
randomisation code broken
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3897778
- UMLS CUI [1,2]
- C1272691
Beschrijving
Randomisation Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0237753
Beschrijving
Investigators Signature
Datatype
text
Alias
- UMLS CUI [1]
- C2346576
Beschrijving
Date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
Beschrijving
name
Datatype
text
Alias
- UMLS CUI [1]
- C0027365
Beschrijving
Medical Monitor’s Signature
Datatype
text
Alias
- UMLS CUI [1]
- C2346576
Beschrijving
Name
Datatype
text
Alias
- UMLS CUI [1]
- C0027365
Beschrijving
Date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
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Serious Adverse Experiences (SAE)
- StudyEvent: ODM
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