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Trials / Not Yet Recruiting

Not Yet RecruitingNCT07195097

Sildosin as a Male Contraceptive Non Hormonal

A Prospective Study to Evaluate the Efficacy of Silodosin 8 mg as an on-Demand, Reversible, Nonhormonal Oral Contraceptive for Males:

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Benha University · Academic / Other
Sex
Male
Age
20 Years
Healthy volunteers
Not accepted

Summary

In all, 200 healthy, sexually active, fertile male candidates will be assigned 100 in silodosin group and 100 in placebo group. Males using other contraceptive methods will be excluded. Follow up data of total spermatozoa per ejaculate, semen volume and Post-ejaculation urinalysis after 2, 6 and 12 weeks of the studied groups will be recorded. The various side effects reported in the study groups after 12 weeks from the start of the study will be recorded.

Conditions

Interventions

TypeNameDescription
DRUGOral intake of sildosinOral intake of sildosin in male non hormonal contraception
OTHEROral intake of placeboIntake of placebo to compare effecacy of other group

Timeline

Start date
2025-09-01
Primary completion
2025-11-01
Completion
2025-12-01
First posted
2025-09-26
Last updated
2025-09-26

Source: ClinicalTrials.gov record NCT07195097. Inclusion in this directory is not an endorsement.