ID

35450

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 (3)
  1. 25/10/18 25/10/18 -
  2. 25/2/19 25/2/19 -
  3. 4/3/19 4/3/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

4 de marzo de 2019

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

SAE Additional/Follow-Up Information

1 formularios  
Administrative data
Descripción

Administrative data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Descripción

Clinical Trial Subject Unique Identifier

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
Centre Number
Descripción

Identifier, Hospitals

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Randomisation Number
Descripción

Randomization, Numbers

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Serious Adverse Event - Additional/Follow-Up Information
Descripción

Serious Adverse Event - Additional/Follow-Up Information

Alias
UMLS CUI-1
C1519255
Use this page to provide any additional details on the SAE not already captured on the previous pages
Descripción

Serious Adverse Event, Details

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C1522508
Investigator's signature
Descripción

confirming that the data on this page is accurate and complete

Tipo de datos

text

Alias
UMLS CUI [1]
C2346576
Investigator's name (print)
Descripción

Investigator Name

Tipo de datos

text

Alias
UMLS CUI [1]
C2826892
Date
Descripción

Date in time

Tipo de datos

date

Alias
UMLS CUI [1]
C0011008
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Similar models

SAE Additional/Follow-Up Information

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Identifier, Hospitals
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Randomization, Numbers
Item
Randomisation Number
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Item Group
Serious Adverse Event - Additional/Follow-Up Information
C1519255 (UMLS CUI-1)
Serious Adverse Event, Details
Item
Use this page to provide any additional details on the SAE not already captured on the previous pages
text
C1519255 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
Investigator Signature
Item
Investigator's signature
text
C2346576 (UMLS CUI [1])
Investigator Name
Item
Investigator's name (print)
text
C2826892 (UMLS CUI [1])
Date in time
Item
Date
date
C0011008 (UMLS CUI [1])
Volver a la parte superior de la página 

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