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NOT YET RECRUITING
NCT07195097
PHASE1

Sildosin as a Male Contraceptive Non Hormonal

Sponsor: Benha University

View on ClinicalTrials.gov

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.

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

Key Details

Gender

MALE

Age Range

20 Years - Any

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2025-09

Completion Date

2025-12

Last Updated

2025-09-26

Healthy Volunteers

No

Interventions

DRUG

Oral intake of sildosin

Oral intake of sildosin in male non hormonal contraception

OTHER

Oral intake of placebo

Intake of placebo to compare effecacy of other group