ID

35450

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 (3)
  1. 25-10-18 25-10-18 -
  2. 25-02-19 25-02-19 -
  3. 04-03-19 04-03-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

4 maart 2019

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

SAE Additional/Follow-Up Information

1 Formulieren  
Administrative data
Beschrijving

Administrative data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Beschrijving

Clinical Trial Subject Unique Identifier

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Centre Number
Beschrijving

Identifier, Hospitals

Datatype

integer

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

Randomization, Numbers

Datatype

integer

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

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
Beschrijving

Serious Adverse Event, Details

Datatype

text

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

confirming that the data on this page is accurate and complete

Datatype

text

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

Investigator Name

Datatype

text

Alias
UMLS CUI [1]
C2826892
Date
Beschrijving

Date in time

Datatype

date

Alias
UMLS CUI [1]
C0011008
Terug naar het begin van de pagina

Similar models

SAE Additional/Follow-Up Information

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

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