ID

32222

Beskrivning

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

Nyckelord

Versioner (3)
  1. 2018-10-24 2018-10-24 -
  2. 2019-01-14 2019-01-14 -
  3. 2019-03-04 2019-03-04 -
Rättsinnehavare

GSK group of companies

Uppladdad den

24 oktober 2018

DOI

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Licens

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

Engelsk

Part 2: Treatment Period - Day 19 - Treatment confirmation

1 Formulär  
Administrative data
Beskrivning

Administrative data

Subject Identifier
Beskrivning

Subject Identifier

Datatyp

integer

Visit Date
Beskrivning

Visit Date

Datatyp

date

Investigational Product
Beskrivning

Investigational Product

Investigational Product
Beskrivning

Investigational Product

Datatyp

text

Planned Timepoint
Beskrivning

Planned Timepoint

Datatyp

text

Date of Dose
Beskrivning

Date of Dose

Datatyp

date

Time of Dose
Beskrivning

Time of Dose

Datatyp

time

Treatment Confirmation
Beskrivning

Treatment Confirmation

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

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

Datatyp

boolean

If NO, record reason(s)
Beskrivning

If NO, record reason(s)

Datatyp

text

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Similar models

Part 2: Treatment Period - Day 19 - Treatment confirmation

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Visit Date
Item
Visit Date
date
Item Group
Investigational Product
Item
Investigational Product
text
Investigational Product
Code List
Investigational Product
CL Item
Dustasteride (1)
CL Item
Dustasteride (2)
Item
Planned Timepoint
text
Planned Timepoint
Code List
Planned Timepoint
CL Item
Day 19 AM (1)
CL Item
Day 19 PM (2)
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
Tillbaka till toppen 

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