ID

25765

Description

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

Keywords

  1. 9/18/17 9/18/17 -
  2. 9/18/17 9/18/17 -
Uploaded on

September 18, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC-ND 3.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :


No comments

In order to download data models you must be logged in. Please log in or register for free.

Death GSK Ropinirole Restless Legs Syndrome 101468

Death GSK Ropinirole Restless Legs Syndrome 101468

Patient Information
Description

Patient Information

Alias
UMLS CUI-1
C1955348
Patient Number
Description

Patient Number

Data type

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Description

Centre Number

Data type

text

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

Form D

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

Complete Serious Adverse Event Form.

Data type

text

Alias
UMLS CUI [1]
C0007465
Date of Death
Description

Date of Death

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1148348
dd-mmm-yyyy
Was a post-mortem carried out?
Description

Autopsy

Data type

boolean

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

Autopsy Specification

Data type

text

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

Investigator's Name

Data type

text

Alias
UMLS CUI [1]
C2826892
Date
Description

Date of Report

Data type

text

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1302584
dd-mmm-yyyy

Similar models

Death GSK Ropinirole Restless Legs Syndrome 101468

Name
Type
Description | Question | Decode (Coded Value)
Data type
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])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial