ID

25759

Beschrijving

Study ID: 101468/191 Clinical Study ID: SKF-101468/191 Study Title:A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Ropinirole in Subjects with Restless Legs Syndrome (RLS) Suffering from Periodic Leg Movements of Sleep (PLMS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Restless Legs Syndrome

Trefwoorden

  1. 17-09-17 17-09-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

17 september 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Form D (Form 23)

GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Form D (Form 23)

General Information
Beschrijving

General Information

Center Number
Beschrijving

Center Number

Datatype

integer

Patient No
Beschrijving

patient number

Datatype

integer

Patient Initials
Beschrijving

Patient Initials

Datatype

text

Form D
Beschrijving

Form D

Certified cause of death
Beschrijving

Certified cause of death

Datatype

text

Date of death
Beschrijving

Date of death

Datatype

date

Was a post-mortem carried out?
Beschrijving

Post-mortem

Datatype

text

If post-mortem was carried out, please summarize findings (include diagnosis)
Beschrijving

Post-mortem findings

Datatype

text

Reporting Physician´s Signature
Beschrijving

Reporting Physician´s Signature

Datatype

text

Date
Beschrijving

Date

Datatype

date

Similar models

GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Form D (Form 23)

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
General Information
Center Number
Item
Center Number
integer
patient number
Item
Patient No
integer
Patient Initials
Item
Patient Initials
text
Item Group
Form D
Certified cause of death
Item
Certified cause of death
text
Date of death
Item
Date of death
date
Item
Was a post-mortem carried out?
text
Code List
Was a post-mortem carried out?
CL Item
No (1)
CL Item
Yes -> If "Yes" please summarize findings (including diagnosis) below (2)
Post-mortem findings
Item
If post-mortem was carried out, please summarize findings (include diagnosis)
text
Reporting Physician´s Signature
Item
Reporting Physician´s Signature
text
Date
Item
Date
date

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