Status:
COMPLETED
Advance Supply of Emergency Contraception Compared to Routine Postpartum Care in Teens
Lead Sponsor:
University of Pennsylvania
Conditions:
Post Partum
Eligibility:
FEMALE
14-19 years
Phase:
PHASE4
Brief Summary
This is a pilot randomized controlled trial to assess the effects of advanced supply of emergency contraception versus routine care in a teen postpartum population. The goals are to assess feasibility...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Female
- English speaking
- Aged 14-19 at enrollment
- Immediately postpartum of a live infant
- Planning to parent the baby
- Desiring to delay another pregnancy for at least one year
- General good health
- Willing and able to follow the study protocol
- Exclusion Criteria
- Allergy to levonorgestrel
- Current substance abuse
- Plans for relocation outside of Philadelphia
Exclusion
Key Trial Info
Start Date :
February 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2010
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00433004
Start Date
February 1 2007
End Date
October 1 2010
Last Update
September 15 2017
Active Locations (1)
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1
Hospital of University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104