ID

25529

Beskrivning

Study ID: 101468/197 Clinical Study ID: SKF-101468/197 Study Title:An open study to compare the PK and tolerability of ropinirole administered as 5 different new formulations with the standard, marketed formulation in healthy volunteers 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: Requip Study Indication : Restless Legs Syndrome

Nyckelord

  1. 2017-09-04 2017-09-04 -
  2. 2017-09-04 2017-09-04 -
  3. 2017-09-05 2017-09-05 -
Uppladdad den

5 september 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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screening physical examination PK and tolerability of ropinirole as 5 new formulations 101468/197

screening physical examination PK and tolerability of ropinirole as 5 new formulations 101468/197

Administrative Data
Beskrivning

Administrative Data

Alias
UMLS CUI-1
C1320722
Focus Panel ID
Beskrivning

focus panel

Datatyp

integer

Alias
UMLS CUI [1]
C3846158
Patient No
Beskrivning

patient number

Datatyp

integer

Alias
UMLS CUI [1]
C1830427
Date
Beskrivning

date

Datatyp

date

Alias
UMLS CUI [1]
C0011008
Physical Examination
Beskrivning

Physical Examination

Alias
UMLS CUI-1
C0031809
Body Area
Beskrivning

body area

Datatyp

text

Alias
UMLS CUI [1]
C1268086
Status
Beskrivning

status

Datatyp

text

Alias
UMLS CUI [1]
C0449438
Description of abnormality
Beskrivning

abnormality

Datatyp

text

Alias
UMLS CUI [1]
C1704258
Investigator
Beskrivning

Investigator

Alias
UMLS CUI-1
C2826892
Investigator's signature
Beskrivning

investigator's signature

Datatyp

text

Alias
UMLS CUI [1]
C2346576
Date
Beskrivning

date

Datatyp

date

Alias
UMLS CUI [1]
C0011008

Similar models

screening physical examination PK and tolerability of ropinirole as 5 new formulations 101468/197

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
focus panel
Item
Focus Panel ID
integer
C3846158 (UMLS CUI [1])
patient number
Item
Patient No
integer
C1830427 (UMLS CUI [1])
date
Item
Date
date
C0011008 (UMLS CUI [1])
Item Group
Physical Examination
C0031809 (UMLS CUI-1)
Item
Body Area
text
C1268086 (UMLS CUI [1])
Code List
Body Area
CL Item
Eyes, ears, nose, mouth, throat (Eyes, ears, nose, mouth, throat)
C0015392 (UMLS CUI-1)
C0013443 (UMLS CUI-3)
C0028429 (UMLS CUI-5)
C0230028 (UMLS CUI-7)
C0031354 (UMLS CUI-9)
(Comment:en)
CL Item
Neck/thyroid (Neck/thyroid)
C0027530 (UMLS CUI-1)
C0040132 (UMLS CUI-3)
(Comment:en)
CL Item
Spine (Spine)
C0037949 (UMLS CUI-1)
(Comment:en)
CL Item
Chest/lungs (Chest/lungs)
C0817096 (UMLS CUI-1)
C0024109 (UMLS CUI-3)
(Comment:en)
CL Item
Heart (Heart)
C0018787 (UMLS CUI-1)
(Comment:en)
CL Item
Vascular system (Vascular system)
C0489903 (UMLS CUI-1)
(Comment:en)
CL Item
Lymph nodes (Lymph nodes)
C0024204 (UMLS CUI-1)
(Comment:en)
CL Item
Abdomen (Abdomen)
C0000726 (UMLS CUI-1)
(Comment:en)
CL Item
Extremities (Extremities)
C0436150 (UMLS CUI-1)
(Comment:en)
CL Item
Nervous system/reflexes (Nervous system/reflexes)
C0027763 (UMLS CUI-1)
C0034929 (UMLS CUI-3)
(Comment:en)
CL Item
Skin (Skin)
CL Item
Musculoskeletal system (Musculoskeletal system)
Item
Status
text
C0449438 (UMLS CUI [1])
Code List
Status
CL Item
Normal (Normal)
CL Item
Abnormal/Pathological (Abnormal/Pathological)
CL Item
Not examined (Not examined)
abnormality
Item
Description of abnormality
text
C1704258 (UMLS CUI [1])
Item Group
Investigator
C2826892 (UMLS CUI-1)
investigator's signature
Item
Investigator's signature
text
C2346576 (UMLS CUI [1])
date
Item
Date
date
C0011008 (UMLS CUI [1])

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