Status:
COMPLETED
Optimizing Postpartum Contraception in Women With Preterm Births
Lead Sponsor:
University of Utah
Conditions:
Method of Contraception
Preterm Birth Recurrence
Eligibility:
FEMALE
14-50 years
Phase:
NA
Brief Summary
The purpose of this study is to examine the effectiveness of focused family planning counseling on the uptake and continuation of highly effective contraceptive methods (defined as the intrauterine de...
Eligibility Criteria
Inclusion
- Women who deliver a premature infant that is between the gestational ages of 24 weeks 0 days and 36 weeks 6 days at our institution.
Exclusion
- Women who have delivered via cesarean section and have also had a sterilization procedure at the time of the cesarean section.
Key Trial Info
Start Date :
April 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2016
Estimated Enrollment :
134 Patients enrolled
Trial Details
Trial ID
NCT01864629
Start Date
April 1 2013
End Date
January 1 2016
Last Update
October 26 2017
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University of Utah Hospital
Salt Lake City, Utah, United States, 84132