A Clinical Feasibility Study to Assess the Performance of a Latex Condom in Healthy Monogamous Couples.

Launched by TITAN CONDOMS, LLC · Oct 8, 2021

Keywords

ClinConnect Summary

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Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Couples not at risk of pregnancy (using alternate contraception).
• • Couples who are past or recent/experienced condom users
• • No known sexually transmitted infections, including HIV/AIDS, gonorrhea, chlamydia, etc.
• • Subjects between 18 to 45 years of age.
• • Monogamous heterosexual couples who agree to practice vaginal sex only during the study.
• • The Titan Size Guide will be used to determine subject eligibility based on the following penis girth measurements
• • Penis girth N64 ≥ 5.8"
• • Penis girth N69 ≥ 6.1"
• Exclusion Criteria:
• • Couples who work for the clinical testing laboratory or who are relatives of staff of the clinical test laboratory or a sponsor of the study.
• • Participants with known allergy to natural rubber latex or material(s) of test condom.
• • Participants with known sensitivity to the residual chemicals used in the manufacturing of natural rubber latex condoms.
• • Couples where one knowingly has a sexually transmitted infection.
• • Male partners have known erectile or ejaculatory dysfunction.
• • Commercial sex workers.
• • Female partner is pregnant or desires to become so while participating in the study.