ID

32232

Descrizione

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

  1. 24/10/18 24/10/18 -
Titolare del copyright

GSK group of companies

Caricato su

24 ottobre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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Bioavailability and Pharmacokinetics of Testosterone with/without Dutasteride - 106218

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

Administrative data
Descrizione

Administrative data

Subject Identifier
Descrizione

Subject Identifier

Tipo di dati

integer

Investigational Product
Descrizione

Investigational Product

Planned Timepoint
Descrizione

Planned Timepoint

Tipo di dati

integer

Investigational Product
Descrizione

Investigational Product

Tipo di dati

text

Date of Dose
Descrizione

Date of Dose

Tipo di dati

date

Time of Dose
Descrizione

Time of Dose

Tipo di dati

time

Treatment Confirmation
Descrizione

Treatment Confirmation

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

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

Tipo di dati

boolean

If NO, record reason(s)
Descrizione

If NO, record reason(s)

Tipo di dati

text

Similar models

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

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Item Group
Investigational Product
Item
Planned Timepoint
integer
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
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

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