ID

32117

Descripción

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

Palabras clave

Versiones (2)
  1. 19/10/18 19/10/18 -
  2. 18/12/18 18/12/18 -
Titular de derechos de autor

GSK group of companies

Subido en

19 de octubre de 2018

DOI

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Licencia

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

Inglés

Pharmacogenetic Research Results (PGx)

1 formularios  
Administrative data
Descripción

Administrative data

Subject Identifier
Descripción

Subject Identifier

Tipo de datos

integer

PGx-Pharmacogenetic Research
Descripción

PGx-Pharmacogenetic Research

Consent for PGx-Pharmacogenetic Research (DNA)
Descripción

Consent for PGx-Pharmacogenetic Research (DNA)

Tipo de datos

text

Has informed consent been obtained for PGx-Pharmacigenetic research?
Descripción

Has informed consent been obtained for PGx-Pharmacigenetic research?

Tipo de datos

boolean

If YES, record the date informed consent obtained for PGx-Pharmacogenetic research
Descripción

If YES, record the date informed consent obtained for PGx-Pharmacogenetic research

Tipo de datos

date

If NO, mark one reason:
Descripción

If NO, mark one reason:

Tipo de datos

text

Blood Sample Collection (DNA)
Descripción

Blood Sample Collection (DNA)

Has a blood sample been collected for PGx-Pharmacocinetic research?
Descripción

Has a blood sample been collected for PGx-Pharmacocinetic research?

Tipo de datos

boolean

If YES, record the date sample taken
Descripción

If YES, record the date sample taken

Tipo de datos

date

Withdrawal of Consent
Descripción

Withdrawal of Consent

Has subject withdrawn consent for PGx-Pharmacogenetic research?
Descripción

Has subject withdrawn consent for PGx-Pharmacogenetic research?

Tipo de datos

boolean

Blood Sample Destruction
Descripción

Blood Sample Destruction

Has a request been made for blood sample destruction?
Descripción

Has a request been made for blood sample destruction?

Tipo de datos

boolean

If YES, mark one reason:
Descripción

If YES, mark one reason:

Tipo de datos

text

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Similar models

Pharmacogenetic Research Results (PGx)

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Item Group
PGx-Pharmacogenetic Research
Consent for PGx-Pharmacogenetic Research (DNA)
Item
Consent for PGx-Pharmacogenetic Research (DNA)
text
Has informed consent been obtained for PGx-Pharmacigenetic research?
Item
Has informed consent been obtained for PGx-Pharmacigenetic research?
boolean
If YES, record the date informed consent obtained for PGx-Pharmacogenetic research
Item
If YES, record the date informed consent obtained for PGx-Pharmacogenetic research
date
Item
If NO, mark one reason:
text
If NO, mark one reason:
Code List
If NO, mark one reason:
CL Item
[1] Subject declined (1)
CL Item
[2] Subject not asked by Investigator (2)
CL Item
[Z] Other, specify__________________________ (3)
Item Group
Blood Sample Collection (DNA)
Has a blood sample been collected for PGx-Pharmacocinetic research?
Item
Has a blood sample been collected for PGx-Pharmacocinetic research?
boolean
If YES, record the date sample taken
Item
If YES, record the date sample taken
date
Item Group
Withdrawal of Consent
Has subject withdrawn consent for PGx-Pharmacogenetic research?
Item
Has subject withdrawn consent for PGx-Pharmacogenetic research?
boolean
Item Group
Blood Sample Destruction
Has a request been made for blood sample destruction?
Item
Has a request been made for blood sample destruction?
boolean
Item
If YES, mark one reason:
text
If YES, mark one reason:
Code List
If YES, mark one reason:
CL Item
[1] Subject requested (1)
CL Item
[2] Screen failure (2)
CL Item
[Z] Other, specify________________________ (3)
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