ID
34531
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)
- 26/10/18 26/10/18 -
- 19/1/19 19/1/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
19 de enero 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
Follow-up - Non-Serious Adverse Events (AE) Form
- StudyEvent: ODM
Descripción
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Descripción
Non-Serious Adverse Event, During, Clinical Trial
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008976
Descripción
Diagnosis only (if known) otherwise sign/symptom
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1518404
Descripción
Non-Serious Adverse Event, Start date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
Descripción
Non-Serious Adverse Event, Adverse Event Outcome
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Descripción
Non-Serious Adverse Event, End date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Descripción
Non-Serious Adverse Event, Frequencies
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Descripción
Maximum Intensity
Tipo de datos
text
Descripción
Non-Serious Adverse Event, Action Taken with Study Treatment
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Descripción
Non-Serious Adverse Event, Withdraw
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2349954
Descripción
Non-Serious Adverse Event, Causations, Experimental
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0085978
- UMLS CUI [1,3]
- C0304229
Similar models
Follow-up - Non-Serious Adverse Events (AE) Form
- StudyEvent: ODM
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C1704758 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])