ID
35978
Description
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 Significant Medical/Surgical History and Physical examination. Both has to be filled in for screening. Physical examination has to be filled in for Follow-up too.
Mots-clés
Versions (1)
- 08/04/2019 08/04/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
8 avril 2019
DOI
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Licence
Creative Commons BY-NC 3.0
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Comparison of pharmacokinetic and tolerability of ropinirole in healthy adults, 101468/198
Significant Medical/Surgical History, Physical examination
- StudyEvent: ODM
Description
Significant Medical/Surgical History
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0489540
Description
If Yes, list below one diagnosis per line. (Please print clearly) Only in the absence of a diagnosis, record the signs and symptoms on separate lines.
Type de données
text
Alias
- UMLS CUI [1]
- C0262926
- UMLS CUI [2]
- C0489540
Description
Diagnosis
Type de données
text
Alias
- UMLS CUI [1]
- C0011900
Description
Investigator Use
Type de données
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0457083
Description
Month/Year
Type de données
partialDate
Alias
- UMLS CUI [1]
- C2316983
Description
Diagnosis from past
Type de données
boolean
Alias
- UMLS CUI [1]
- C0455458
Description
Ongoing disease
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0549178
- UMLS CUI [1,2]
- C0012634
Description
Physical Examination
Alias
- UMLS CUI-1
- C0031809
Description
day month year
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
"Physical Examination should be performed and any relevant findings must be described on the Medical History form (for findings of the past), or on the Baseline Sign/Symptom form (for findings presently occurring, events existing prior to drug administration). IMPORTANT: these findings, or events, must have a complete starting date that is at, or before, the date of the assessment (so that these are clearly pre-treatment findings, or events)." If any clinically significant abnormalities are present, DO NOT INCLUDE the subject.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C0243095
Description
Findings, specification
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0243095
- UMLS CUI [1,2]
- C2348235
Description
Other findings
Type de données
text
Alias
- UMLS CUI [1]
- C1335151
Similar models
Significant Medical/Surgical History, Physical examination
- StudyEvent: ODM
C0489540 (UMLS CUI-2)
C0489540 (UMLS CUI [2])
C0457083 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
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