ID

32232

Beschrijving

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

Trefwoorden

Versies (1)
  1. 24-10-18 24-10-18 -
Houder van rechten

GSK group of companies

Geüploaded op

24 oktober 2018

DOI

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Licentie

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

Engels

Part 2: Repeat Dose Phase - Day 21 - Treatment confirmation

1 Formulieren  
Administrative data
Beschrijving

Administrative data

Subject Identifier
Beschrijving

Subject Identifier

Datatype

integer

Investigational Product
Beschrijving

Investigational Product

Planned Timepoint
Beschrijving

Planned Timepoint

Datatype

integer

Investigational Product
Beschrijving

Investigational Product

Datatype

text

Date of Dose
Beschrijving

Date of Dose

Datatype

date

Time of Dose
Beschrijving

Time of Dose

Datatype

time

Treatment Confirmation
Beschrijving

Treatment Confirmation

Did the subject receive the correct treatment (e.g, treatment which the subject was assigned to) during this dosing interval?
Beschrijving

Did the subject receive the correct treatment (e.g, treatment which the subject was assigned to) during this dosing interval?

Datatype

boolean

If NO, record reason(s)
Beschrijving

If NO, record reason(s)

Datatype

text

Terug naar het begin van de pagina

Similar models

Part 2: Repeat Dose Phase - Day 21 - Treatment confirmation

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Item Group
Investigational Product
Item
Planned Timepoint
integer
Planned Timepoint
Code List
Planned Timepoint
CL Item
Day 20 AM (1)
CL Item
Day 20 AM (2)
CL Item
Day 20 PM (3)
CL Item
Day 20 PM (4)
Item
Investigational Product
text
Investigational Product
Code List
Investigational Product
CL Item
Dustasteride (1)
CL Item
Testosterone (2)
CL Item
Dustasteride (3)
CL Item
Testosterone (4)
Date of Dose
Item
Date of Dose
date
Time of Dose
Item
Time of Dose
time
Item Group
Treatment Confirmation
Did the subject receive the correct treatment (e.g, treatment which the subject was assigned to) during this dosing interval?
Item
Did the subject receive the correct treatment (e.g, treatment which the subject was assigned to) during this dosing interval?
boolean
If NO, record reason(s)
Item
text
Terug naar het begin van de pagina 

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