A 3-way Crossover Clinical Investigation to Assess the Performance of Two Different Sized Polyurethane Condoms Versus a Latex Condom in Healthy Monogamous Couples.

NARecruitingINTERVENTIONAL
Enrollment

600

Participants

Timeline

Start Date

August 23, 2024

Primary Completion Date

May 19, 2025

Study Completion Date

May 19, 2025

Conditions
Contraception
Interventions
DEVICE

Polyurethane (PU) male condom-Test condom 1

A minimum of 5 condoms (maximum 7 condoms) of each condom type will be provided to couples to be used during vaginal intercourse over a maximum 5-week period (assessment period). Couples will repeat the assessment period for each of the 3 condom types.

DEVICE

Polyurethane (PU) male condom-Test condom 2

A minimum of 5 condoms (maximum 7 condoms) of each condom type will be provided to couples to be used during vaginal intercourse over a maximum 5-week period (assessment period). Couples will repeat the assessment period for each of the 3 condom types.

DEVICE

Natural Rubber Latex (NRL) male condom- Control condom

A minimum of 5 condoms (maximum 7 condoms) of each condom type will be provided to couples to be used during vaginal intercourse over a maximum 5-week period (assessment period). Couples will repeat the assessment period for each of the 3 condom types.

Trial Locations (3)

90010

RECRUITING

Essential Access Health-Berkeley, Berkeley

90017

RECRUITING

Essential Access Health -Los Angeles, Los Angeles

98005

RECRUITING

Essential Acess Health- Seattle, Seattle

All Listed Sponsors
collaborator

Novotech (Australia) Pty Limited

INDUSTRY

lead

Reckitt Benckiser Healthcare (UK) Limited

INDUSTRY

NCT06557499 - A 3-way Crossover Clinical Investigation to Assess the Performance of Two Different Sized Polyurethane Condoms Versus a Latex Condom in Healthy Monogamous Couples. | Biotech Hunter | Biotech Hunter