drugset / Trial / NCT01299116

Long-Acting Reversible Contraception

NCT01299116

Phase 4 Completed 916 enrolled FHI 360
RandomizedParallel-groupOpen-labelPrevention

Summary

In the proposed study, women aged 18-29 seeking oral or injectable contraception will be offered an opportunity to try LARC instead; the FDA-approved options include two types of intrauterine products and one type of subdermal contraceptive implant. Over a 24 month period, the experiences of LARC users will be compared to the experiences of those opting for their initial short-acting method.

Timeline

Start
2011-12
Primary completion
2016-06
Completion
2016-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Etonogestrel Unknown 68 mg Subcutaneous
Subject Levonorgestrel Small molecule 52 mg Other
Subject medroxyprogesterone acetate Other / unclassified 104 mg Other
Subject medroxyprogesterone acetate Other / unclassified 150 mg Other

Indications

No indication recorded.