Phase 4
N=7
Intrauterine Contraceptive Device (IUD) Placement at Time of C-Section
Contraception
Bottom Line
View on ClinicalTrials.gov: NCT00733278 ↗Enrolled (actual)
7
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcome: Primary: Successful Retention of IUD — 7 participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- Copper IUD ( ParaGard Intrauterine Contraceptive Device) (Device)
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
- Primary completion
- Sep 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Successful Retention of IUD |
7 | — |
| SECONDARY Visibility Within the Vagina of IUD Strings at All Times. |
7 | — |
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 feasible and acceptable to women seeking long-term contraception.
Eligibility Criteria
Inclusion Criteria
- Pregnant woman
- Requires elective C-section
- Desires long-term contraception
Exclusion Criteria
- Contraindications to copper IUD
Data sourced from ClinicalTrials.gov (NCT00733278). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.