Clinical Trials Directory

Trials / Completed

CompletedNCT04134130

The Role of Follicle Stimulating Hormone in Advanced Prostate Cancer

Case Control Study Regarding the Role of Follicle Stimulating Hormone in Chemically Castrated Young Men

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Lund University · Academic / Other
Sex
Male
Age
20 Years – 30 Years
Healthy volunteers
Accepted

Summary

In order to elucidate if FSH can have testosterone like effects, samples from young, non-smoking healthy volunteers, with normal body mass index, and with pharmacologically induced gonadotropin deficiency will be studied regarding their capacity to induce prostate specific antigen (PSA), which normally is regulated by testosterone.

Detailed description

Normally, prostate specific antigen (PSA), which is a marker for prostate disease and progression, is exclusively produced in response to testosterone. In order to elucidate if follicle stimulating hormone (FSH) can have testosterone like effects, samples from n=30 non-smoking healthy volunteers, 20-30 years of age and with normal body mass index (20-25) with pharmacologically induced gonadotropin deficiency will be studied. The men are currently recruited and during 5 weeks undergoing: 1. Pharmacologically induced gonadotropin deficiency w 1-3; 2. FSH-treatment of 50% (group A), w 1-5; 3. Testosterone (T) treatment of all (group A and B) w 4-5; 4. End and follow up after 5 weeks. A subcutaneous injection with the GnRH antagonist degarelix (240 mg¸ Ferring GmbH Wittland, Kiel, Germany) results in drop of both FSH and LH-induced testosterone. Half of the men will get recombinant FSH (300 IU; Gonal-f, Merck Serrono S.A. Aubonne, Schweiz) back, whereas 50% will not. Three weeks thereafter, the full spectrum of FSH dependent changes occur and are reflected in blood. From this occasion testosterone (Nebido, Ferring GmbH Wittland, Kiel, Germany) will be given to all participants to diminish the side-effects of the castration. Blood samples are collected at start, after 3 wks and after 5 wks. At that point also a follow up is undertaken. This experimental design will provide samples from each individual during normal conditions, during castration, and after a standardised dose of FSH.

Conditions

Interventions

TypeNameDescription
DRUGDegarelix 120 MG [Firmagon]Two doses of degarelix, 240 mg, subcutaneously once, at study start.
DRUGGonal F RFF Pen 900 UNT Per 1.5 ML Pen InjectorGonal-f 300 IU subcutaneously 3 times per week for 5 weeks.
DRUGTestosterone UndecanoateOne dose 1000 mg testosterone once, after 3 weeks.

Timeline

Start date
2019-09-16
Primary completion
2019-12-20
Completion
2019-12-31
First posted
2019-10-22
Last updated
2020-01-22

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT04134130. Inclusion in this directory is not an endorsement.