Sildosin as a Male Contraceptive Non Hormonal

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexMale
Age20+
SponsorBenha University

About this trial

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.

Eligibility criteria

Qualifiers

male sexually active

Disqualifiers

male on oral contraceptives Male with female partner on contraceptives

Trial design

Treatments tested in this trial

  • Oral intake of sildosin
  • Oral intake of placebo

Treatment groups

200 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators