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National Institutes of Child Health and Human Development / A multi-center, randomized study of the efficacy of ulipristal acetate (UPA) 30 mg, levonorgestrel (LNG) 1.5 mg, and LNG 3.0 mg for emergency contraception (EC) in women with weight 80 kg
A Study of Emergency Contraception in Women with Weight Greater Than or Equal To 176 lbs.
| Sponsor: | The National Institutes of Health NIH - National Institutes of Child Health and Human Development |
| Enrolling: | Female Patients Only |
| Study Length: | 1 Months |
| Clinic Visits: | 1 |
| IRB Number: | AAAR8722 |
| U.S. Govt. ID: | NCT03537768 |
| Contact: | Yessica Estrella Vanterpool: 212-305-8031 / ye2193@cumc.columbia.edu |
Additional Study Information:
Did you have unprotected sex? Do you weigh at least 176 pounds? This clinical trial is an experimental research study using a new dose of emergency contraception or morning-after pill. You may qualify if you: Are a premenopausal, healthy woman between the ages of 18 and 40. Weigh more than 176 pounds. Have an intact uterus with at least one ovary. Have regular menstrual cycles. If you qualify, you will: Receive a free investigational emergency contraceptive pill. Comply with protocol requirements, including taking an oral medication. Attend approximately 2 clinic visits and receive follow up phone calls over approximately one month. Receive financial compensation for completing the study.
This study is closed
