ID

35500

Beschrijving

Study ID: 101468/194 Clinical Study ID: 101468/194 Study Title: A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy and Safety 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 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome

Trefwoorden

Versies (1)
  1. 06-03-19 06-03-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

6 maart 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Ropinirole in Patients with Restless Legs Syndrome (Study ID: 101468/194)

Engels

Medical Procedures

1 Formulieren  
  1. StudyEvent: ODM
    1. Medical Procedures
Administrative data
Beschrijving

Administrative data

Alias
UMLS CUI-1
C1320722
Centre Number
Beschrijving

Study Coordinating Center, Identification number

Datatype

integer

Alias
UMLS CUI [1,1]
C2825181
UMLS CUI [1,2]
C1300638
Patient Number
Beschrijving

Clinical Trial Subject Unique Identifier

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Patient Initials
Beschrijving

Person Initials

Datatype

text

Alias
UMLS CUI [1]
C2986440
Medical Procedures
Beschrijving

Medical Procedures

Alias
UMLS CUI-1
C0199171
Have any non-medication, therapeutic, diagnostic or surgical procedures been performed since the last visit?
Beschrijving

If ‘Yes’, please record details below using standard medical terminology (Please print clearly)

Datatype

boolean

Alias
UMLS CUI [1]
C0199171
Procedure
Beschrijving

Medical procedure

Datatype

text

Alias
UMLS CUI [1]
C0199171
Indication
Beschrijving

Medical procedure, Indication

Datatype

text

Alias
UMLS CUI [1,1]
C0199171
UMLS CUI [1,2]
C3146298
Procedure Start Date
Beschrijving

Medical procedure, Start Date

Datatype

date

Alias
UMLS CUI [1,1]
C0199171
UMLS CUI [1,2]
C0808070
Procedure End Date
Beschrijving

Medical procedure, End Date

Datatype

date

Alias
UMLS CUI [1,1]
C0199171
UMLS CUI [1,2]
C0806020
Terug naar het begin van de pagina

Similar models

Medical Procedures

1 Formulieren
  1. StudyEvent: ODM
    1. Medical Procedures
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Study Coordinating Center, Identification number
Item
Centre Number
integer
C2825181 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Clinical Trial Subject Unique Identifier
Item
Patient Number
integer
C2348585 (UMLS CUI [1])
Person Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Item Group
Medical Procedures
C0199171 (UMLS CUI-1)
Medical procedure
Item
Have any non-medication, therapeutic, diagnostic or surgical procedures been performed since the last visit?
boolean
C0199171 (UMLS CUI [1])
Medical procedure
Item
Procedure
text
C0199171 (UMLS CUI [1])
Medical procedure, Indication
Item
Indication
text
C0199171 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
Medical procedure, Start Date
Item
Procedure Start Date
date
C0199171 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Medical procedure, End Date
Item
Procedure End Date
date
C0199171 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

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