Phase 4
Completed N=7
Intrauterine Contraceptive Device (IUD) Placement at Time of C-Section
Source: ClinicalTrials.gov NCT00733278 ↗Enrolled (actual)
7
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcomePrimary: Successful Retention of IUD — 7 participants
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Successful Retention of IUD |
7 | — |
| SECONDARY Visibility Within the Vagina of IUD Strings at All Times. |
7 | — |
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. Informational only — not medical advice.