Status:
COMPLETED
Copper Intrauterine Device (IUD) Insertion at Cesarean Delivery
Lead Sponsor:
Albert Einstein College of Medicine
Conditions:
Intrauterine Device Expulsion
Eligibility:
FEMALE
18-50 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to determine the expulsion rates of copper Intrauterine Devices (IUDs) placed at time of Cesarean Delivery.
Detailed Description
This was a prospective clinical study with 90 patients undergoing cesarean section. After delivery of the placenta, a ParaGard® copper T380A IUD was inserted through the hysterotomy site. IUD placemen...
Eligibility Criteria
Inclusion
- singleton gestation
- greater than 35 weeks gestation
- speaks English or Spanish
- desires IUD for contraception
- undergoing a cesarean delivery
Exclusion
- evidence of chorioamnionitis
- history of chlamydia within this pregnancy
Key Trial Info
Start Date :
August 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2010
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT01439802
Start Date
August 1 2008
End Date
May 1 2010
Last Update
April 7 2023
Active Locations (2)
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1
Jacobi Medical Center
The Bronx, New York, United States, 10461
2
Montefiore Medical Center, Weiler Division
The Bronx, New York, United States, 10461