Status:
COMPLETED
Intrauterine Contraceptive Device (IUD) Placement at Time of C-Section
Lead Sponsor:
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Conditions:
Contraception
Eligibility:
FEMALE
18-50 years
Phase:
PHASE4
Brief Summary
This is a pilot study of up to 10 women, which will test the hypothesis that the placement of copper IUDs through the uterine incision at the time of uncomplicated elective C-section is technically fe...
Detailed Description
Women will be enrolled in this study during late prenatal care. Consent for placement of the IUD will be verified prior to elective C-section. After removal of the placenta, the copper IUD will be pla...
Eligibility Criteria
Inclusion
- Pregnant woman
- Requires elective C-section
- Desires long-term contraception
Exclusion
- Contraindications to copper IUD
Key Trial Info
Start Date :
November 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2008
Estimated Enrollment :
7 Patients enrolled
Trial Details
Trial ID
NCT00733278
Start Date
November 1 2007
End Date
September 1 2008
Last Update
August 11 2014
Active Locations (1)
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1
Los Angeles BRI
Torrance, California, United States, 90502