ID

36124

Descrizione

Study ID: 101468/198 Clinical Study ID: 101468/198 Study Title:An open, randomised, crossover, healthy volunteer study to compare the PK and tolerability of ropinirole as 3 different new formulations with the standard marketed formulation and to study the effects of a high fat meal on a new formulation Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Restless Legs Syndrome The Study consists of a Screening, 5 Sessions each with 2 days and a Follow-up. This document contains the Follow-Up Physical Examination form. It has to be filled in for follow-up.

Keywords

  1. 16/04/19 16/04/19 -
Titolare del copyright

GlaxoSmithKline

Caricato su

16 aprile 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Comparison of pharmacokinetic and tolerability of ropinirole in healthy adults, 101468/198

Follow-Up Physical Examination

Administrative data
Descrizione

Administrative data

Alias
UMLS CUI-1
C1320722
Subject No.
Descrizione

Subject No.

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Panel ID
Descrizione

Panel ID

Tipo di dati

text

Alias
UMLS CUI [1]
C3846158
Physical Examination
Descrizione

Physical Examination

Alias
UMLS CUI-1
C0031809
Date of Assessment:
Descrizione

day month year

Tipo di dati

date

Alias
UMLS CUI [1]
C2985720
Time of Assessment
Descrizione

00.00-23:59

Tipo di dati

time

Alias
UMLS CUI [1]
C2826761
Has there been any change from the last examination (screening)?
Descrizione

Change from last examination

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C0443172
If there has been any change from the last examination, please record in this item. Any clinically relevant worsening since the last exam must be record on the Adverse Events page.
Descrizione

Change, specification

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C0034869

Similar models

Follow-Up Physical Examination

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Subject No.
Item
Subject No.
text
C2348585 (UMLS CUI [1])
Panel ID
Item
Panel ID
text
C3846158 (UMLS CUI [1])
Item Group
Physical Examination
C0031809 (UMLS CUI-1)
Date of Assessment
Item
Date of Assessment:
date
C2985720 (UMLS CUI [1])
Time of Assessment
Item
Time of Assessment
time
C2826761 (UMLS CUI [1])
Item
Has there been any change from the last examination (screening)?
text
C0031809 (UMLS CUI [1,1])
C0443172 (UMLS CUI [1,2])
Code List
Has there been any change from the last examination (screening)?
CL Item
Yes (Y)
CL Item
No (N)
Change, specification
Item
If there has been any change from the last examination, please record in this item. Any clinically relevant worsening since the last exam must be record on the Adverse Events page.
text
C0031809 (UMLS CUI [1,1])
C0034869 (UMLS CUI [1,2])

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

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