ID

25765

Descripción

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 Death

Palabras clave

Versiones (2)
  1. 18/9/17 18/9/17 -
  2. 18/9/17 18/9/17 -
Subido en

18 de septiembre de 2017

DOI

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Licencia

Creative Commons BY-NC-ND 3.0
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Death GSK Ropinirole Restless Legs Syndrome 101468

Inglés

Death GSK Ropinirole Restless Legs Syndrome 101468

1 formularios  
Patient Information
Descripción

Patient Information

Alias
UMLS CUI-1
C1955348
Patient Number
Descripción

Patient Number

Tipo de datos

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Descripción

Centre Number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Form D
Descripción

Form D

Alias
UMLS CUI-1
C0011065
Certified Cause of Death:
Descripción

Complete Serious Adverse Event Form.

Tipo de datos

text

Alias
UMLS CUI [1]
C0007465
Date of Death
Descripción

Date of Death

Tipo de datos

date

Unidades de medida
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1148348
dd-mmm-yyyy
Was a post-mortem carried out?
Descripción

Autopsy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004398
Was a post-mortem carried out? If 'YES', please summarize findings (include diagnosis):
Descripción

Autopsy Specification

Tipo de datos

text

Alias
UMLS CUI [1]
C2348235
Physician's Signature
Descripción

Investigator's Name

Tipo de datos

text

Alias
UMLS CUI [1]
C2826892
Date
Descripción

Date of Report

Tipo de datos

text

Unidades de medida
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1302584
dd-mmm-yyyy
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Similar models

Death GSK Ropinirole Restless Legs Syndrome 101468

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Patient Information
C1955348 (UMLS CUI-1)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
text
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Item Group
Form D
C0011065 (UMLS CUI-1)
Cause of Death
Item
Certified Cause of Death:
text
C0007465 (UMLS CUI [1])
Date of Death
Item
Date of Death
date
C1148348 (UMLS CUI [1])
Autopsy
Item
Was a post-mortem carried out?
boolean
C0004398 (UMLS CUI [1])
Autopsy Specification
Item
Was a post-mortem carried out? If 'YES', please summarize findings (include diagnosis):
text
C2348235 (UMLS CUI [1])
Investigator's Name
Item
Physician's Signature
text
C2826892 (UMLS CUI [1])
Date of Report
Item
Date
text
C1302584 (UMLS CUI [1])
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