ID

26386

Description

Study Part: Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2). An open-label, up-titration study to assess the dose proportionality of ropinirole controlled release (CR) and to demonstrate the bioequivalence of ropinirole CR (1 x 8 mg) compared to the ropinirole CR (4 x 2 mg) in Parkinson's Disease patients not receiving other dopaminergic therapies. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Phase: phase 2. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP,Zygara. Study Indication: Parkinson Disease. Study ID: 101468/165. Clinical Study ID: 101468/165

Mots-clés

  1. 16/10/2017 16/10/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

16 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2) Ropinirole Parkinson Disease 101468/165

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2)

ADVERSE EVENTS & CONCOMITANT MEDICATIONS
Description

ADVERSE EVENTS & CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C0877248
UMLS CUI-3
C2347852
Patient Number
Description

Patient Number

Type de données

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Description

Centre Number

Type de données

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Visit Date
Description

Visit Date

Type de données

date

Alias
UMLS CUI [1]
C1320303
Has the subject experienced any Adverse Events?
Description

Adverse Events

Type de données

boolean

Alias
UMLS CUI [1]
C0877248
Has the subject taken any Concomitant medications?
Description

Concomitant medications

Type de données

boolean

Alias
UMLS CUI [1]
C2347852

Similar models

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2)

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
ADVERSE EVENTS & CONCOMITANT MEDICATIONS
C0877248 (UMLS CUI-1)
C2347852 (UMLS CUI-3)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Adverse Events
Item
Has the subject experienced any Adverse Events?
boolean
C0877248 (UMLS CUI [1])
Concomitant medications
Item
Has the subject taken any Concomitant medications?
boolean
C2347852 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

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