ID
24978
Descripción
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
Palabras clave
Versiones (3)
- 23/8/17 23/8/17 -
- 23/8/17 23/8/17 -
- 4/9/17 4/9/17 -
Subido en
23 de agosto de 2017
DOI
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Licencia
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
Descripción
1- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
4- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
12- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
24- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0439568
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
QUERY FOR ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Descripción
If YES, please record in the Adverse Events section below. Spontaneously reported or observed Adverse Events should be recorded in the Adverse Events section.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0877248
Descripción
ADVERSE EVENTS
Alias
- UMLS CUI-1
- C0877248
Descripción
ADVERSE EVENT
Alias
- UMLS CUI-1
- C0877248
Descripción
If serious, set a tickmark in the field below. Otherwise leave it empty.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1710066
Descripción
24-hour clock
Tipo de datos
datetime
Alias
- UMLS CUI [1]
- C2697888
- UMLS CUI [2]
- C2697889
Descripción
if ongoing, please leave blank 24-hour clock
Tipo de datos
datetime
Alias
- UMLS CUI [1]
- C2697886
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C1522314
Descripción
intensity of adverse event
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1710066
Descripción
relationship to drug
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0277579
Descripción
change of medication
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0580105
Descripción
If "Yes", record on Concomitant Medication form.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0087111
Descripción
If intermittent, record number of episodes.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Descripción
outcome of adverse event
Tipo de datos
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])