ID
24978
Beskrivning
Study ID: 101468/166 Clinical Study ID: SKF-101468/166 Study Title: A Phase II, randomised, double-blind, active-controlled, dose-escalation study to determine the maximum well-tolerated starting dose of a new formulation of ropinirole in Parkinson's Disease patients not receiving other dopaminergic therapies 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: Parkinson Disease
Nyckelord
Versioner (3)
- 2017-08-23 2017-08-23 -
- 2017-08-23 2017-08-23 -
- 2017-09-04 2017-09-04 -
Uppladdad den
23 augusti 2017
DOI
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Licens
Creative Commons BY-NC 3.0 Legacy
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adverse events determination of the maximum well-tolerated starting dose of ropinirole in Parkinson's Disease 101468/166
adverse events determination of the maximum well-tolerated starting dose of ropinirole in Parkinson's Disease 101468/166
Beskrivning
1- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
4- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
12- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
24- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Beskrivning
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Beskrivning
ADVERSE EVENT
Alias
- UMLS CUI-1
- C0877248
Beskrivning
If serious, set a tickmark in the field below. Otherwise leave it empty.
Datatyp
text
Alias
- UMLS CUI [1]
- C1710066
Beskrivning
24-hour clock
Datatyp
datetime
Alias
- UMLS CUI [1]
- C2697888
- UMLS CUI [2]
- C2697889
Beskrivning
if ongoing, please leave blank 24-hour clock
Datatyp
datetime
Alias
- UMLS CUI [1]
- C2697886
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C1522314
Beskrivning
intensity of adverse event
Datatyp
integer
Alias
- UMLS CUI [1]
- C1710066
Beskrivning
relationship to drug
Datatyp
integer
Alias
- UMLS CUI [1]
- C0277579
Beskrivning
change of medication
Datatyp
integer
Alias
- UMLS CUI [1]
- C0580105
Beskrivning
If "Yes", record on Concomitant Medication form.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0087111
Beskrivning
If intermittent, record number of episodes.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Beskrivning
outcome of adverse event
Datatyp
integer
Alias
- UMLS CUI [1]
- C1705586
Similar models
adverse events determination of the maximum well-tolerated starting dose of ropinirole in Parkinson's Disease 101468/166
C0439568 (UMLS CUI-2)
C0439568 (UMLS CUI-2)
C0439568 (UMLS CUI-2)
C0439568 (UMLS CUI-2)
C2697889 (UMLS CUI [2])
C0877248 (UMLS CUI [2,1])
C1522314 (UMLS CUI [2,2])
C0087111 (UMLS CUI [1,2])
C0750729 (UMLS CUI [1,2])