Overview
Immediate Versus Delayed Insertion of Implanon in Postpartum Adolescents
Status:
Completed
Completed
Trial end date:
2013-01-01
2013-01-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The specific aim of this study is to evaluate whether insertion of a long-acting contraceptive implant in postpartum adolescents prior to hospital discharge increases use of this highly effective contraception during the first twelve months postpartum among adolescents who elect Implanon® as their preferred method of contraception. Additionally, this study aims to compare the acceptability of bleeding in postpartum adolescents who have an etonogestrel contraceptive implant prior to discharge versus those with insertion at the six week postpartum visit. The investigators will evaluate the acceptability of bleeding rather than collect prospective diaries because the investigators feel subjective perceptions of bleeding impact contraceptive continuation more than quantitative differences in bleeding.Phase:
Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Medical University of South CarolinaCollaborators:
American College of Obstetricians and Gynecologists
BayerTreatments:
Contraceptive Agents
Desogestrel
Etonogestrel
Criteria
Inclusion Criteria:- ages 15-21
- women
- english or spanish speaking
- less than 120 hours post partum
Exclusion Criteria:
- women who are breastfeeding
- contraindications to Implanon® insertion including current or prior thrombo-embolic
disease, liver disease, hypersensitivity to components of Implanon®, or are using
medications such as rifampin, phenytoin, or carbamazepine that increase metabolism of
steroid hormones.
- indicate unwillingness to continue follow-up for one year.