ID
29114
Beschreibung
Study ID: 101468/249 Clinical Study ID: 101468/249 Study Title: A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363857 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: N/A 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; Restless Legs Syndrome (RLS)
Stichworte
Versionen (1)
- 26.02.18 26.02.18 -
Rechteinhaber
GlaxoSmithKline (GSK)
Hochgeladen am
26. Februar 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Clinical Study, Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS), Study ID: 101468/249, NCT00363857
Study medication and compliance record
- StudyEvent: ODM
Beschreibung
Study medication
Alias
- UMLS CUI-1
- C0013227
- UMLS CUI-2
- C0304229
- UMLS CUI-3
- C0008976
- UMLS CUI-4
- C0035258
Beschreibung
Study Medication Week No.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0439230
Beschreibung
If ’Yes’, please complete the Dose Reductions due to AE on page 95. Do not continue on this page for this visit.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1707814
Beschreibung
Dose level
Datentyp
integer
Alias
- UMLS CUI [1]
- C0178602
Beschreibung
Date of first dose
Datentyp
date
Alias
- UMLS CUI [1]
- C3173309
Beschreibung
Date of last dose
Datentyp
date
Alias
- UMLS CUI [1]
- C1762893
Beschreibung
Number of tablets dispensed
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0805077
- UMLS CUI [1,2]
- C0039225
Beschreibung
Number of tablets returned
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2699071
- UMLS CUI [1,2]
- C0039225
Beschreibung
Interruption
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1512900
Beschreibung
Dose Reduction due to adverse experiences
Alias
- UMLS CUI-1
- C1707814
- UMLS CUI-2
- C0559546
Beschreibung
Study Med. Week No.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0439230
Beschreibung
Dose level
Datentyp
integer
Alias
- UMLS CUI [1]
- C0178602
Beschreibung
Date of first dose
Datentyp
date
Alias
- UMLS CUI [1]
- C3173309
Beschreibung
Date of last dose
Datentyp
date
Alias
- UMLS CUI [1]
- C1762893
Beschreibung
Number of tablets dispensed
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0805077
- UMLS CUI [1,2]
- C0039225
Beschreibung
Number of tablets returned
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2699071
- UMLS CUI [1,2]
- C0039225
Beschreibung
Interruption
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1512900
Beschreibung
Study Med. Week No.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0439230
Beschreibung
Medication Label
Datentyp
text
Alias
- UMLS CUI [1]
- C0013227
Beschreibung
Medication Labels
Alias
- UMLS CUI-1
- C0013227
Beschreibung
Study Med. Week No.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0439230
Beschreibung
Medication Label
Datentyp
text
Alias
- UMLS CUI [1]
- C0013227
Ähnliche Modelle
Study medication and compliance record
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0304229 (UMLS CUI-2)
C0008976 (UMLS CUI-3)
C0035258 (UMLS CUI-4)
C0039225 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C1512900 (UMLS CUI [1,2])
C0559546 (UMLS CUI-2)
C0439230 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C1512900 (UMLS CUI [1,2])