Status:
COMPLETED
Postplacental Intrauterine Device Insertion: A Mixed Methods Assessment of Women's Experience
Lead Sponsor:
University of New Mexico
Collaborating Sponsors:
Society of Family Planning
Conditions:
Contraception
Eligibility:
FEMALE
18+ years
Brief Summary
The primary objective of this mixed methods pilot study is to understand women's experiences with postplacental intrauterine device (IUD) insertion through postpartum semi-structured interviews. For s...
Detailed Description
Postplacental IUD insertion following vaginal or cesarean delivery is as effective in preventing pregnancy as interval insertion, and it is utilized more often in other countries such as China, Mexico...
Eligibility Criteria
Inclusion
- English-speaking or Spanish-speaking only (SSO) women
- Women who express a desire to have an IUD inserted immediately following anticipated vaginal delivery.
Exclusion
- Unanticipated cesarean delivery
- Chorioamnionitis
- Significant postpartum hemorrhage (estimated blood loss requiring intervention beyond standard therapy and not resolved within approximately 10 minutes)
- Third or fourth degree obstetric vaginal laceration
- Manual extraction of the placenta
- Untreated gonorrhea, chlamydia and/or trichomoniasis
- Known or suspected distorted uterine cavity
- Current use of controlled substances for chronic pain management
- Current substance abuse/ addiction.
Key Trial Info
Start Date :
November 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
March 1 2015
Estimated Enrollment :
135 Patients enrolled
Trial Details
Trial ID
NCT02312726
Start Date
November 1 2013
End Date
March 1 2015
Last Update
April 4 2016
Active Locations (1)
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1
University of New Mexico Health Sciences Center
Albuquerque, New Mexico, United States, 87131