Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07143279

Testosterone Supplementation in Patients in Best Supportive Care: Impact on Quality of Life

Status
Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Jules Bordet Institute · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a monocentric, single-arm prospective pilot study that will enrol hypogonadal (testosterone \< 231 ng/dL) male subjects in best supportive care, with no further therapeutic options and no need for resuscitation. Currently, testosterone formulations for intramuscular (IM) injection and subcutaneous injection as well as for oral and transdermal administration have been approved for androgen therapy. To date, injectable testosterone is the most commonly used formulation. To increase serum testosterone levels to the physiological range IM injections of testosterone every 2-3 weeks are required, which lead to supraphysiological peaks shortly after administration, followed by a sharp fall in levels thereafter. Testosterone levels before the next injection are frequently in the hypogonadal range. For this reason, Sustanon 250® (1 ml, IM) will be administered on day 0 after confirmation of hypogonadism by blood test and then every 15 days in this trial given the limited life expectancy of the subjects and to maximise the effect and benefit of testosterone supplementation. The Edmonton questionnaire and ADL questionnaire will be completed before the injection on day 0 and then every 15 days at the time of injection until subject's death or if a subject is discontinued from the study treatment/procedures for any other reasons than death. In parallel, the EQ-5D-3L questionnaire will be completed by a family member or a proxy.

Conditions

Interventions

TypeNameDescription
DRUGSustanon 250Sustanon 250® (1 ml, IM) every 10 days

Timeline

Start date
2026-02-11
Primary completion
2026-11-01
Completion
2027-11-01
First posted
2025-08-27
Last updated
2026-02-13

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT07143279. Inclusion in this directory is not an endorsement.