ID

35500

Beskrivning

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

Nyckelord

Versioner (1)
  1. 2019-03-06 2019-03-06 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

6 mars 2019

DOI

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Licens

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

Engelsk

Medical Procedures

1 Formulär  
  1. StudyEvent: ODM
    1. Medical Procedures
Administrative data
Beskrivning

Administrative data

Alias
UMLS CUI-1
C1320722
Centre Number
Beskrivning

Study Coordinating Center, Identification number

Datatyp

integer

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

Clinical Trial Subject Unique Identifier

Datatyp

integer

Alias
UMLS CUI [1]
C2348585
Patient Initials
Beskrivning

Person Initials

Datatyp

text

Alias
UMLS CUI [1]
C2986440
Medical Procedures
Beskrivning

Medical Procedures

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

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

Datatyp

boolean

Alias
UMLS CUI [1]
C0199171
Procedure
Beskrivning

Medical procedure

Datatyp

text

Alias
UMLS CUI [1]
C0199171
Indication
Beskrivning

Medical procedure, Indication

Datatyp

text

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

Medical procedure, Start Date

Datatyp

date

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

Medical procedure, End Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0199171
UMLS CUI [1,2]
C0806020
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Similar models

Medical Procedures

1 Formulär
  1. StudyEvent: ODM
    1. Medical Procedures
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

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