ID

35500

Description

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

Keywords

Versions (1)
  1. 3/6/19 3/6/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

March 6, 2019

DOI

To request one please log in.

License

Creative Commons BY-NC 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.

Back to model comments
Itemgroup comments for :

Item comments for :

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

Ropinirole in Patients with Restless Legs Syndrome (Study ID: 101468/194)

English

Medical Procedures

1 forms  
  1. StudyEvent: ODM
    1. Medical Procedures
Administrative data
Description

Administrative data

Alias
UMLS CUI-1
C1320722
Centre Number
Description

Study Coordinating Center, Identification number

Data type

integer

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

Clinical Trial Subject Unique Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
Patient Initials
Description

Person Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Medical Procedures
Description

Medical Procedures

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

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

Data type

boolean

Alias
UMLS CUI [1]
C0199171
Procedure
Description

Medical procedure

Data type

text

Alias
UMLS CUI [1]
C0199171
Indication
Description

Medical procedure, Indication

Data type

text

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

Medical procedure, Start Date

Data type

date

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

Medical procedure, End Date

Data type

date

Alias
UMLS CUI [1,1]
C0199171
UMLS CUI [1,2]
C0806020
Back to the top of the page

Similar models

Medical Procedures

1 forms
  1. StudyEvent: ODM
    1. Medical Procedures
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
Back to the top of the page 

Contact

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

Fields marked with * are required.

Help

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