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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02102646
Other study ID # kk2013 MRI
Secondary ID
Status Completed
Phase Phase 4
First received March 27, 2014
Last updated October 27, 2015
Start date April 2014
Est. completion date October 2015

Study information

Verified date October 2015
Source Herlev Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if androgen deprivation therapy in men with prostate cancer increases hepatic fat content and changes visceral/subcutaneous fat distribution.


Description:

This is a substudy of the ongoing randomized trial entitled: Metabolic Changes Due to Iatrogenic Hypogonadism in Patients With Prostate Cancer: Orchiectomy vs. Triptorelin (EudraCT number: 2013-002553-29). 20 consecutive patients are anticipated to participate regardless of assignment to either orchiectomy or triptorelin.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date October 2015
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Eligible for inclusion are patients who are included in the already ongoing Randomised trial entitled: Metabolic Changes Due to Iatrogenic Hypogonadism in Patients With Prostate Cancer: Orchiectomy vs. Triptorelin (EudraCT number: 2013-002553-29)

Exclusion Criteria:

- Implanted devices or foreign metallic bodies incompatible with Magnetic Resonance Imaging.

- claustrophobia

- Severe Psychiatric disease

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Triptorelin
Androgen deprivation therapy by Pamorelin 22,5mg/24 weeks administered intramuscularly.
Procedure:
Orchiectomy
Androgen deprivation therapy by bilateral subcapsular orchiectomy

Locations

Country Name City State
Denmark Herlev Hospital Herlev

Sponsors (1)

Lead Sponsor Collaborator
Herlev Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in hepatic fat content Change in hepatic fat content measured by Magnetic Resonance Spectroscopy At baseline (within 4 weeks of commencement of androgen deprivation therapy) and after 24 weeks No
Secondary Change in visceral/subcutaneous fat mass Changes in visceral and subcutaneous fat mass measured by Magnetic Resonance Imaging. At baseline (within 4 weeks of commencement of androgen deprivation therapy) and after 24 weeks No
Secondary Correlation between Hepatic fat content and baseline androgen status To investigate possible correlation between androgen status before commencing androgen deprivation therapy and hepatic fat content at baseline. Androgen status measured before commencement of androgen deprivation therapy (ADT), hepatic fat content measured at baseline (within 1 month of commencing androgen deprivation therapy) No
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