ID

25765

Beschrijving

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

Trefwoorden

Versies (2)
  1. 18-09-17 18-09-17 -
  2. 18-09-17 18-09-17 -
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18 september 2017

DOI

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Licentie

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

Engels

Death GSK Ropinirole Restless Legs Syndrome 101468

1 Formulieren  
Patient Information
Beschrijving

Patient Information

Alias
UMLS CUI-1
C1955348
Patient Number
Beschrijving

Patient Number

Datatype

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Beschrijving

Centre Number

Datatype

text

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

Form D

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

Complete Serious Adverse Event Form.

Datatype

text

Alias
UMLS CUI [1]
C0007465
Date of Death
Beschrijving

Date of Death

Datatype

date

Maateenheden
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1148348
dd-mmm-yyyy
Was a post-mortem carried out?
Beschrijving

Autopsy

Datatype

boolean

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

Autopsy Specification

Datatype

text

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

Investigator's Name

Datatype

text

Alias
UMLS CUI [1]
C2826892
Date
Beschrijving

Date of Report

Datatype

text

Maateenheden
  • 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 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

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