ID
25762
Beschreibung
Study ID: 101468/207 Clinical Study ID: SKF-101468/207 Study Title:A double-blind, randomized, placebo-controlled, parallel-group study to investigate the tolerability of a dose-escalating regimen of ropinirole in patients suffering from Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Restless Legs Syndrome AE Section
Stichworte
Versionen (1)
- 18.09.17 18.09.17 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
18. September 2017
DOI
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Creative Commons BY-NC-ND 3.0
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AE Section GSK Ropinirole Restless Legs Syndrome 101468
AE Section GSK Ropinirole Restless Legs Syndrome 101468
- StudyEvent: ODM
Beschreibung
Adverse Event - Please note any SERIOUS events should NOT be recorded on this page, but on the SERIOUS ADVERSE EVENT pages provided. Record any Adverse event (using standard medical terminology) observed or elicited as a result of spontaneous reporting by patient 'How are you feeling' (pre-dose) and at subsequent schedules intervals post dose: 'Since you were last asked have you felt unwell or different from usual?'
Alias
- UMLS CUI-1
- C0877248
Beschreibung
Adverse Event
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0877248
Beschreibung
Adverse Event: Specification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C2348235
Beschreibung
Onset Date
Datentyp
date
Maßeinheiten
- dd-mmm-yyyy
Alias
- UMLS CUI [1]
- C0574845
Beschreibung
Onset Time
Datentyp
time
Maßeinheiten
- 24hr:min
Alias
- UMLS CUI [1]
- C0449244
Beschreibung
End Date
Datentyp
date
Maßeinheiten
- dd-mmm-yyyy
Alias
- UMLS CUI [1]
- C0806020
Beschreibung
End Time
Datentyp
time
Maßeinheiten
- 24hr:min
Alias
- UMLS CUI [1]
- C1522314
Beschreibung
Adverse Event Outcome
Datentyp
text
Alias
- UMLS CUI [1]
- C1705586
Beschreibung
Event Course
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Beschreibung
Number of Episodes
Datentyp
float
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C4086638
Beschreibung
Intensity
Datentyp
text
Beschreibung
Action Taken
Datentyp
text
Alias
- UMLS CUI [1]
- C2826626
Beschreibung
Relationship
Datentyp
text
Alias
- UMLS CUI [1]
- C0439849
Beschreibung
Corrective Therapy
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0087111
Beschreibung
Withdrawal due to Adverse Event
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C1519255
Beschreibung
Adverse Event Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2697888
Ähnliche Modelle
AE Section GSK Ropinirole Restless Legs Syndrome 101468
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C4086638 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])