ID

24531

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: Follow-Up Physical Examination, b-HCG Pregnancy Test, Vital Signs, 12-Lead ECG Monitoring

Keywords

Versions (1)
  1. 8/5/17 8/5/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 5, 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 Follow-Up Physical Examination, Serum b-HCB Pregnancy Test, Vital Signs, 12-Lead ECG Monitoring

English

GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Follow-Up Physical Examination, Serum b-HCB Pregnancy Test, Vital Signs, 12-Lead ECG Monitoring

1 forms  
Physical Examination
Description

Physical Examination

Alias
UMLS CUI-1
C0031809
Date
Description

physical examination date

Data type

date

Alias
UMLS CUI [1]
C2826643
Time
Description

physical examination time

Data type

time

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

Record below. Any clinically relevant worsening since the last exam must be recorded on the Adverse Events page.

Data type

boolean

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C0443172
Has there been any change from the last examination (Screening)?
Description

Record below. Any clinically relevant worsening since the last exam must be recorded on the Adverse Events page.

Data type

text

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C0443172
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: Date and time of pregnancy test
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:
Description

If POSITIVE, withdraw the subject from the study.

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
Vital Signs
Description

Vital Signs

Alias
UMLS CUI-1
C0518766
Study Time
Description

study time

Data type

text

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0040223
Date
Description

vital signs date

Data type

date

Alias
UMLS CUI [1]
C2826644
Actual Time
Description

vital signs time

Data type

time

Alias
UMLS CUI [1]
C2826762
Systolic BP
Description

systolic blood pressure

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
Diastolic BP
Description

diastolic blood pressure

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1]
C0428883
mmHg
HR
Description

heart rate

Data type

integer

Measurement units
  • bpm
Alias
UMLS CUI [1]
C0018810
bpm
Respiratory Rate
Description

respiratory rate

Data type

text

Alias
UMLS CUI [1]
C0231832
12-Lead ECG Monitoring
Description

12-Lead ECG Monitoring

Alias
UMLS CUI-1
C0430456
Study Time
Description

study time

Data type

text

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0040223
Date
Description

ecg date

Data type

date

Alias
UMLS CUI [1,1]
C0013798
UMLS CUI [1,2]
C0011008
Actual Time
Description

ecg time

Data type

time

Alias
UMLS CUI [1,1]
C0013798
UMLS CUI [1,2]
C0040223
Heart Rate
Description

heart rate

Data type

integer

Measurement units
  • bpm
Alias
UMLS CUI [1]
C0018810
bpm
PR
Description

pr duration

Data type

float

Measurement units
  • msec
Alias
UMLS CUI [1]
C1880446
msec
QRS
Description

qrs duration

Data type

float

Measurement units
  • msec
Alias
UMLS CUI [1]
C0429025
msec
QT
Description

qt duration

Data type

float

Measurement units
  • msec
Alias
UMLS CUI [1]
C1880452
msec
QTC
Description

qtc interval

Data type

float

Measurement units
  • msec
Alias
UMLS CUI [1]
C0855331
msec
ECG Normal?
Description

ecg normal

Data type

boolean

Alias
UMLS CUI [1]
C0522054
Comments
Description

ecg comment

Data type

text

Alias
UMLS CUI [1,1]
C1623258
UMLS CUI [1,2]
C0947611
Back to the top of the page

Similar models

GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Follow-Up Physical Examination, Serum b-HCB Pregnancy Test, Vital Signs, 12-Lead ECG Monitoring

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Physical Examination
C0031809 (UMLS CUI-1)
physical examination date
Item
Date
date
C2826643 (UMLS CUI [1])
physical examination time
Item
Time
time
C2826761 (UMLS CUI [1])
physical examination change
Item
Has there been any change from the last examination (Screening)?
boolean
C0031809 (UMLS CUI [1,1])
C0443172 (UMLS CUI [1,2])
physical examination change
Item
Has there been any change from the last examination (Screening)?
text
C0031809 (UMLS CUI [1,1])
C0443172 (UMLS CUI [1,2])
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: Date and time of pregnancy test
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:
text
C0032976 (UMLS CUI [1])
pregnancy test result
Code List
If YES, please indicate date and time of test and result:
CL Item
Positive (Positive)
CL Item
Negative (Negative)
laboratory name
Item
Laboratory name, if applicable
text
C1882331 (UMLS CUI [1])
Item Group
Vital Signs
C0518766 (UMLS CUI-1)
Item
Study Time
text
C2348563 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
study time
Code List
Study Time
CL Item
Follow-up (Follow-up)
CL Item
Unscheduled (Unscheduled)
vital signs date
Item
Date
date
C2826644 (UMLS CUI [1])
vital signs time
Item
Actual Time
time
C2826762 (UMLS CUI [1])
systolic blood pressure
Item
Systolic BP
integer
C0871470 (UMLS CUI [1])
diastolic blood pressure
Item
Diastolic BP
integer
C0428883 (UMLS CUI [1])
heart rate
Item
HR
integer
C0018810 (UMLS CUI [1])
respiratory rate
Item
Respiratory Rate
text
C0231832 (UMLS CUI [1])
Item Group
12-Lead ECG Monitoring
C0430456 (UMLS CUI-1)
Item
Study Time
text
C2348563 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
study time
Code List
Study Time
CL Item
Follow-up (Follow-up)
CL Item
Unscheduled (Unscheduled)
ecg date
Item
Date
date
C0013798 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
ecg time
Item
Actual Time
time
C0013798 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
heart rate
Item
Heart Rate
integer
C0018810 (UMLS CUI [1])
pr duration
Item
PR
float
C1880446 (UMLS CUI [1])
qrs duration
Item
QRS
float
C0429025 (UMLS CUI [1])
qt duration
Item
QT
float
C1880452 (UMLS CUI [1])
qtc interval
Item
QTC
float
C0855331 (UMLS CUI [1])
ecg normal
Item
ECG Normal?
boolean
C0522054 (UMLS CUI [1])
ecg comment
Item
Comments
text
C1623258 (UMLS CUI [1,1])
C0947611 (UMLS CUI [1,2])
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