Birth Control Clinical Trials

Consider a research study for uterine fibroids. The Asteroid Studies are research studies evaluating the safety and effectiveness of an investigational oral medication for uterine fibroids.

Northern California Research is currently enrolling participants for a birth control study. The purpose of this study is to assess the effectiveness of a new form of birth control in preventing pregnancy. The study medication is a new, non-hormonal, birth control designed to maintain the pH of the vagina and ...

Birth Control Study

HWC Women's Research Center is conducting a clinical research study of an investigational birth control. You may qualify for: No-cost birth control Study-related care Reimbursement for time and travel

Birth control is any method used to prevent pregnancy. There are many different methods of birth control. This particular method of contraception is a small patch that sticks to your skin to prevent pregnancy.

Currently we have the following studies: Birth Control/ Contraceptive Vaginal Atrophy Pain During Intercourse Dysplasia Endometriosis Pap Smear Mammogram Bone Density Osteoporosis Nocturia Uterine Fibroids Uterine Bleeding Post Menopausal Studies HPV STD Hot Flashes

The EPIC study will evaluate whether Implanon or Mirena IUD are effective at preventing pregnancy after their FDA approved durations. Study participation includes a baseline phone survey and phone surveys every 6 months for about 36 months. A $20 gift card is provided for each completed survey. Risks and benefits ...

We are currently offering an open-label study to evaluate the efficacy and safety of a combination oral contraceptive regimen for the prevention of pregnancy in women. Give us a call or email to see if you qualify.

Women's Health Research Ctr. is conducting a clinical research study of an investigational oral medication for birth control. Patient Inclusion Criteria: Females ages 18-40 years of age, sexually active, and have regular menstrual cycles are eligible for participation in a 12 month study for birth control. Patient Exclusion Criteria: Must ...

The total duration of the study for each participant is expected to be approximately 39 months: including screening and enrollment (up to 30 days to meet enrollment criteria), 37 months of participation, and a post-removal follow up telephone call 17 days post-removal. After enrollment, subject visits occur at 6 weeks, ...