ID

24158

Description

Study ID: 100716 Clinical Study ID: NKP100716 Study Title: An open label repeat dose study to investigate the effect of GW597599 (15 mg) and paroxetine (10 mg) given in combination for 15 days on the pharmacokinetics of midazolam and dextromethorphan in healthy male and female 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: vestipitant Trade Name: paroxetine and vestipitant Study Indication: Depressive Disorder and Anxiety Disorders Documentation part: Treatment Period 1 Laboratory Collections 1

Keywords

Versions (1)
  1. 7/26/17 7/26/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 26, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Treatment Period 1 Laboratory Collections 1

English

GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Treatment Period 1 Laboratory Collections

1 forms  
Urinanalysis
Description

Urinanalysis

Alias
UMLS CUI-1
C0042014
Exact date and time of urine sampling
Description

urine sampling date and time

Data type

datetime

Alias
UMLS CUI [1,1]
C0200354
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Comments:
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Are there CLINICALLY SIGNIFICANT ABNORMAL values? If Yes, please record diagnosis on the Adverse Events page.
Description

urinanalysis normal

Data type

boolean

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0205307
Drug Screening (Urine)
Description

Drug Screening (Urine)

Alias
UMLS CUI-1
C0202274
Exact date and time of sampling
Description

urine sampling date and time

Data type

datetime

Alias
UMLS CUI [1,1]
C0200354
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Where there any contra-indicated drugs detected? If YES, please record all the relevant contra-indicated drugs below.
Description

drug screening positive

Data type

boolean

Alias
UMLS CUI [1,1]
C0202274
UMLS CUI [1,2]
C1446409
Type of drug
Description

drug type

Data type

text

Alias
UMLS CUI [1]
C0457591
Comment
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Alcohol Breath Test
Description

Alcohol Breath Test

Alias
UMLS CUI-1
C0202306
Exact date and time of test
Description

alcohol breath test date and time

Data type

datetime

Alias
UMLS CUI [1,1]
C0202306
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Alcohol breath test positive or negative? If positive please withdraw the subject from the study.
Description

alcohol breath test

Data type

text

Alias
UMLS CUI [1]
C0202306
Urine Cotinine Test
Description

Urine Cotinine Test

Alias
UMLS CUI-1
C1697737
Exact date and time of test
Description

If positive please withdraw from the study.

Data type

datetime

Alias
UMLS CUI [1,1]
C1697737
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Serum b-HCG Pregnancy Test (Females Only)
Description

Serum b-HCG Pregnancy Test (Females Only)

Alias
UMLS CUI-1
C0430060
Was a pregnancy test carried out?
Description

pregnancy test

Data type

boolean

Alias
UMLS CUI [1]
C0430060
If NO, please specify reason
Description

pregnancy test reason

Data type

text

Alias
UMLS CUI [1]
C0430060
If YES, please indicate date and time of test and result:
Description

pregnancy test date and time

Data type

datetime

Alias
UMLS CUI [1,1]
C0430060
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
If YES, please indicate date and time of test and result: If Positive, withdraw the subject from the study.
Description

pregnancy test result

Data type

text

Alias
UMLS CUI [1]
C0032976
Laboratory name, if applicable
Description

Ensure result is included on laboratory report

Data type

text

Alias
UMLS CUI [1]
C1882331
Back to the top of the page

Similar models

GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Treatment Period 1 Laboratory Collections

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Urinanalysis
C0042014 (UMLS CUI-1)
urine sampling date and time
Item
Exact date and time of urine sampling
datetime
C0200354 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
comment
Item
Comments:
text
C0947611 (UMLS CUI [1])
urinanalysis normal
Item
Are there CLINICALLY SIGNIFICANT ABNORMAL values? If Yes, please record diagnosis on the Adverse Events page.
boolean
C0042014 (UMLS CUI [1,1])
C0205307 (UMLS CUI [1,2])
Item Group
Drug Screening (Urine)
C0202274 (UMLS CUI-1)
urine sampling date and time
Item
Exact date and time of sampling
datetime
C0200354 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
drug screening positive
Item
Where there any contra-indicated drugs detected? If YES, please record all the relevant contra-indicated drugs below.
boolean
C0202274 (UMLS CUI [1,1])
C1446409 (UMLS CUI [1,2])
drug type
Item
Type of drug
text
C0457591 (UMLS CUI [1])
comment
Item
Comment
text
C0947611 (UMLS CUI [1])
Item Group
Alcohol Breath Test
C0202306 (UMLS CUI-1)
alcohol breath test date and time
Item
Exact date and time of test
datetime
C0202306 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item
Alcohol breath test positive or negative? If positive please withdraw the subject from the study.
text
C0202306 (UMLS CUI [1])
alcohol breath test
Code List
Alcohol breath test positive or negative? If positive please withdraw the subject from the study.
CL Item
Positive (Positive)
CL Item
Negative (Negative)
Item Group
Urine Cotinine Test
C1697737 (UMLS CUI-1)
urine cotinine test date and time
Item
Exact date and time of test
datetime
C1697737 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item Group
Serum b-HCG Pregnancy Test (Females Only)
C0430060 (UMLS CUI-1)
pregnancy test
Item
Was a pregnancy test carried out?
boolean
C0430060 (UMLS CUI [1])
pregnancy test reason
Item
If NO, please specify reason
text
C0430060 (UMLS CUI [1])
pregnancy test date and time
Item
If YES, please indicate date and time of test and result:
datetime
C0430060 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item
If YES, please indicate date and time of test and result: If Positive, withdraw the subject from the study.
text
C0032976 (UMLS CUI [1])
pregnancy test result
Code List
If YES, please indicate date and time of test and result: If Positive, withdraw the subject from the study.
CL Item
Positive (Positive)
CL Item
Negative (Negative)
laboratory name
Item
Laboratory name, if applicable
text
C1882331 (UMLS CUI [1])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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