Study Details
Testing Ovaprene® as a Method of Birth Control
(IRB#: IRB_00170641)
The study device, Ovaprene, is a possible new method of birth control. The study will test the device to see if it will help people and is safe. Participants assigned female at birth will use the device. Standard-of-care counseling will be provided before using the device. Participants will record study activity in an electronic diary. Participation requires attending in-person visits at the study clinic. Full participation lasts about 15 months. Medical tests will be done to track the health of participants.
- Female Only
- Over 18 years old
- Healthy Volunteers
- In Person
- Unpaid
Who can participate?
Gender: Female Only
Age: Over 18 years old
Volunteers: Healthy Volunteers
Location: In Person
Inclusion Criteria
- Ages 18 to 40 years old
- General good health
- Sexually active people assigned female at birth, at risk for pregnancy, and desiring birth control
- In a relationship with a person assigned male at birth who meets the study criteria
- Willing to stop current use of birth control
Exclusion Criteria
- Pregnant or breastfeeding an infant 6 months or younger
- Allergy to a part of Ovaprene
- History of infertility (failure of pregnancy)
- History of severe or chronic medical or mental health disorder impacting participation
- Known current alcohol or drug abuse
Will I be paid for my time?
No
IRB#: IRB_00170641
PI: David Turok
Department: OBSTETRICS/GYNECOLOGY DEPT OP
Approval Date: 2024-02-14 18:16:00
Specialties: OB/Gyn, General