Status:
WITHDRAWN
Intrauterine Device (IUD) Placement at the Time of Cesarean Section
Lead Sponsor:
University of Kentucky
Collaborating Sponsors:
Duramed Research
Conditions:
Intrauterine Device Placement
Eligibility:
FEMALE
18-40 years
Brief Summary
To evaluate the continuation of the Copper IUD at one year after placement through the cesarean incision into the uterus at the time of cesarean section.
Eligibility Criteria
Inclusion
- Desire an IUD post-partum and are willing to use the copper IUD.
- They will also need to be patients at one of our OBGYN clinics at the university of Kentucky.
Exclusion
- Post-partum hemorrhage,
- Chorioamnionitis (or a fever \>101 at the time of cesarean),
- Women on antibiotic or immunosuppressive therapies,
- Cervical dilation \> 5 cm at the time of c-section, OR
- Excessive intraoperative blood loss.
- Also women with contraindications to a copper IUD: Wilson's disease, unusual uterine shape or known uterine anomaly.
Key Trial Info
Start Date :
August 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
July 1 2010
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00986089
Start Date
August 1 2008
End Date
July 1 2010
Last Update
December 22 2016
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