ID

32050

Description

Study ID: 106218 Clinical Study ID: TDC106218 Study Title: Study On Bioavailability And Pharmacokinetics Of Various Doses Of Testosterone Administered With And Without Dutasteride  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: testosterone Trade Name: Andropatch,Androderm Study Indication: Hypogonadism, Male

Keywords

Versions (2)
  1. 10/16/18 10/16/18 -
  2. 1/30/19 1/30/19 -
Copyright Holder

GSK group of companies

Uploaded on

October 16, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Bioavailability and Pharmacokinetics of Testosterone with/without Dutasteride - 106218

English

24-Hour Haemotology Laboratory Result Data - Day 1

1 forms  
Haemotology
Description

Haemotology

Subject Identifier
Description

Subject Identifier

Data type

integer

Date sample taken
Description

Date sample taken

Data type

date

Time sample taken
Description

Time sample taken

Data type

time

Has the subject fasted?
Description

Has the subject fasted?

Data type

boolean

Haemotology Test
Description

Haemotology Test

Hematocrit
Description

Hematocrit

Data type

integer

Haemoglobin
Description

Haemoglobin

Data type

integer

Red Blood Cell Count
Description

Red Blood Cell Count

Data type

integer

MCV
Description

MCV

Data type

integer

NCH
Description

NCH

Data type

integer

MCHC
Description

MCHC

Data type

integer

Platelet Count
Description

Platelet Count

Data type

integer

White Blood Cell Count
Description

White Blood Cell Count

Data type

integer

Neutrophils (Absolute)
Description

Neutrophils (Absolute)

Data type

integer

Neutrophils
Description

Neutrophils

Data type

integer

Measurement units
  • %
%
Lymphocytes (Absolute)
Description

Lymphocytes (Absolute)

Data type

integer

Lymphocytes
Description

Lymphocytes

Data type

integer

Measurement units
  • %
%
Monocytes (Absolute)
Description

Monocytes (Absolute)

Data type

integer

Monocytes
Description

Monocytes

Data type

integer

Measurement units
  • %
%
Eosinophils (Absolute)
Description

Eosinophils (Absolute)

Data type

integer

Eosinophils
Description

Eosinophils

Data type

integer

Measurement units
  • %
%
Basophils (Absolute)
Description

Basophils (Absolute)

Data type

integer

Basophils
Description

Basophils

Data type

integer

Measurement units
  • %
%
If the laboratory results meet the protocol definition of an adverse event, record the details on the Non-Serious Adverse Events page or Serious Adverse Event page.
Description

If the laboratory results meet the protocol definition of an adverse event, record the details on the Non-Serious Adverse Events page or Serious Adverse Event page.

Data type

text

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Similar models

24-Hour Haemotology Laboratory Result Data - Day 1

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Haemotology
Subject Identifier
Item
Subject Identifier
integer
Date sample taken
Item
Date sample taken
date
Time sample taken
Item
Time sample taken
time
Has the subject fasted?
Item
Has the subject fasted?
boolean
Item Group
Haemotology Test
Hematocrit
Item
Hematocrit
integer
Haemoglobin
Item
Haemoglobin
integer
Red Blood Cell Count
Item
Red Blood Cell Count
integer
MCV
Item
MCV
integer
NCH
Item
NCH
integer
MCHC
Item
MCHC
integer
Platelet Count
Item
Platelet Count
integer
White Blood Cell Count
Item
White Blood Cell Count
integer
Neutrophils (Absolute)
Item
Neutrophils (Absolute)
integer
Neutrophils
Item
Neutrophils
integer
Lymphocytes (Absolute)
Item
Lymphocytes (Absolute)
integer
Lymphocytes
Item
Lymphocytes
integer
Monocytes (Absolute)
Item
Monocytes (Absolute)
integer
Monocytes
Item
Monocytes
integer
Eosinophils (Absolute)
Item
Eosinophils (Absolute)
integer
Eosinophils
Item
Eosinophils
integer
Basophils (Absolute)
Item
Basophils (Absolute)
integer
Basophils
Item
Basophils
integer
If the laboratory results meet the protocol definition of an adverse event, record the details on the Non-Serious Adverse Events page or Serious Adverse Event page.
Item
If the laboratory results meet the protocol definition of an adverse event, record the details on the Non-Serious Adverse Events page or Serious Adverse Event page.
text
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