ID

27541

Descripción

Study Part: Clinical Data Review Form. An open-label, up-titration study to assess the dose proportionality of ropinirole controlled release (CR) and to demonstrate the bioequivalence of ropinirole CR (1 x 8 mg) compared to the ropinirole CR (4 x 2 mg) in Parkinson's Disease patients not receiving other dopaminergic therapies. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Phase: phase 2. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP,Zygara. Study Indication: Parkinson Disease. Study ID: 101468/165. Clinical Study ID: 101468/165

Palabras clave

Versiones (1)
  1. 19/11/17 19/11/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

19 de noviembre de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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Clinical Data Review Form Ropinirole Parkinson Disease 101468/165

Inglés

Clinical Data Review Form

1 formularios  
Administrative Documentation
Descripción

Administrative Documentation

Alias
UMLS CUI-1
C1320722
To: Data Management @
Descripción

Data Management

Tipo de datos

text

Alias
UMLS CUI [1]
C0011005
Drug ID:
Descripción

Drug ID

Tipo de datos

text

Alias
UMLS CUI [1,1]
C4256366
UMLS CUI [1,2]
C0600091
Protocol No:
Descripción

Protocol No

Tipo de datos

text

Alias
UMLS CUI [1,1]
C3274381
UMLS CUI [1,2]
C1711341
Inv.Name/Centre No:
Descripción

Centre No

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0805701
Patient No:
Descripción

Patient No

Tipo de datos

text

Alias
UMLS CUI [1]
C1830427
From: Medical Dept. @
Descripción

Medical Dept.

Tipo de datos

text

Alias
UMLS CUI [1]
C1553421
CRF Module(s):
Descripción

CRF Module

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1516308
UMLS CUI [1,2]
C1709061
Review comments:
Descripción

Review comments:

Alias
UMLS CUI-1
C0947611
1) Serious AE:
Descripción

Serious AE

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519255
AE Text:
Descripción

Adverse events

Tipo de datos

text

Alias
UMLS CUI [1]
C0877248
2) Missing pages:
Descripción

Missing pages

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1548329
To follow:
Descripción

To follow

Tipo de datos

text

Alias
UMLS CUI [1]
C1522577
3) Missing data:
Descripción

Missing data

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1705492
UMLS CUI [1,2]
C1511726
To follow:
Descripción

To follow

Tipo de datos

text

Alias
UMLS CUI [1]
C1522577
Page No:
Descripción

Page No

Tipo de datos

integer

Alias
UMLS CUI [1]
C0237753
Unobtainable:
Descripción

Unobtainable

Tipo de datos

text

Alias
UMLS CUI [1]
C2046401
4) Protocol Violations:
Descripción

Protocol Violations

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1709750
Page No:
Descripción

Page No

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0814891
UMLS CUI [1,2]
C1704732
5) DRQ replies:
Descripción

DRQ replies

Tipo de datos

text

6) Other comments:
Descripción

other

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0205394
Page No:
Descripción

Page No

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0814891
UMLS CUI [1,2]
C1704732
Monitor:
Descripción

Monitor

Tipo de datos

text

Alias
UMLS CUI [1]
C1521743
Name:
Descripción

Name

Tipo de datos

text

Alias
UMLS CUI [1]
C0027365
Date of review:
Descripción

Date of review

Tipo de datos

date

Alias
UMLS CUI [1,1]
C3166277
UMLS CUI [1,2]
C0011008
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Similar models

Clinical Data Review Form

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Documentation
C1320722 (UMLS CUI-1)
Data Management
Item
To: Data Management @
text
C0011005 (UMLS CUI [1])
Drug ID
Item
Drug ID:
text
C4256366 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Protocol No
Item
Protocol No:
text
C3274381 (UMLS CUI [1,1])
C1711341 (UMLS CUI [1,2])
Centre No
Item
Inv.Name/Centre No:
text
C1301943 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
Patient No
Item
Patient No:
text
C1830427 (UMLS CUI [1])
Medical Dept.
Item
From: Medical Dept. @
text
C1553421 (UMLS CUI [1])
CRF Module
Item
CRF Module(s):
text
C1516308 (UMLS CUI [1,1])
C1709061 (UMLS CUI [1,2])
Item Group
Review comments:
C0947611 (UMLS CUI-1)
Serious AE
Item
1) Serious AE:
boolean
C1519255 (UMLS CUI [1])
Adverse events
Item
AE Text:
text
C0877248 (UMLS CUI [1])
Missing pages
Item
2) Missing pages:
boolean
C1548329 (UMLS CUI [1])
To follow
Item
To follow:
text
C1522577 (UMLS CUI [1])
Missing data
Item
3) Missing data:
boolean
C1705492 (UMLS CUI [1,1])
C1511726 (UMLS CUI [1,2])
To follow
Item
To follow:
text
C1522577 (UMLS CUI [1])
Page No
Item
Page No:
integer
C0237753 (UMLS CUI [1])
Unobtainable
Item
Unobtainable:
text
C2046401 (UMLS CUI [1])
Protocol Violations
Item
4) Protocol Violations:
boolean
C1709750 (UMLS CUI [1])
Page No
Item
Page No:
integer
C0814891 (UMLS CUI [1,1])
C1704732 (UMLS CUI [1,2])
DRQ replies
Item
5) DRQ replies:
text
other
Item
6) Other comments:
boolean
C0205394 (UMLS CUI [1])
Page No
Item
Page No:
integer
C0814891 (UMLS CUI [1,1])
C1704732 (UMLS CUI [1,2])
Monitor
Item
Monitor:
text
C1521743 (UMLS CUI [1])
Name
Item
Name:
text
C0027365 (UMLS CUI [1])
Date of review
Item
Date of review:
date
C3166277 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
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