ID

27191

Description

Study ID: 101468/188 Clinical Study ID: SKF-101468/188 Study Title:A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of 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: Parkinson Disease Module: Medical Procedures

Mots-clés

Versions (1)
  1. 03/11/2017 03/11/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

3 novembre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

Anglais

Medical Procedures

1 Formulaires  
  1. StudyEvent: ODM
    1. Medical Procedures
Medical Procedures
Description

Medical Procedures

Alias
UMLS CUI-1
C0199171
UMLS CUI-2
C0087111
UMLS CUI-3
C0430022
UMLS CUI-4
C0543467
Have any non-medication, therapeutic, diagnostic or surgical procedures been performed since the last clinic visit (non-PSG)? All indications for procedures should be recorded in the Adverse Experience and/or SAE section as appropriate.
Description

If "Yes", please record details below using standard medical terminology.

Type de données

boolean

Alias
UMLS CUI [1]
C0199171
UMLS CUI [2]
C0087111
UMLS CUI [3]
C0430022
UMLS CUI [4]
C0543467
Procedure
Description

Procedure

Type de données

text

Alias
UMLS CUI [1,1]
C0199171
UMLS CUI [1,2]
C0332307
Indication for procedure
Description

Indication for procedure

Type de données

text

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

Procedure Start Date

Type de données

date

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

Procedure End Date

Type de données

date

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

Medical Procedures

1 Formulaires
  1. StudyEvent: ODM
    1. Medical Procedures
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Medical Procedures
C0199171 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0430022 (UMLS CUI-3)
C0543467 (UMLS CUI-4)
Medical Procedures
Item
Have any non-medication, therapeutic, diagnostic or surgical procedures been performed since the last clinic visit (non-PSG)? All indications for procedures should be recorded in the Adverse Experience and/or SAE section as appropriate.
boolean
C0199171 (UMLS CUI [1])
C0087111 (UMLS CUI [2])
C0430022 (UMLS CUI [3])
C0543467 (UMLS CUI [4])
Procedure
Item
Procedure
text
C0199171 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Indication for procedure
Item
Indication for procedure
text
C0199171 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
Procedure Start Date
Item
Procedure Start Date
date
C0199171 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Procedure End Date
Item
Procedure End Date
date
C0199171 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Retour au début de la page 

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