Trials / Completed
CompletedNCT03780985
Post-placental Intrauterine Device Insertion During Cesarean Section
Hang-up Versus Non-fixation Technique for Immediate Post-placental Intrauterine Device Insertion During Cesarean Section
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 118 (actual)
- Sponsor
- Assiut University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
Effective, reversible postpartum contraception decreases the chance of rapid repeat pregnancy and poor perinatal outcome in a subsequent pregnancy especially in women delivered by cesarean section.The traditional 6-week postpartum visits not evidenced based and may not meet patient needs, particularly with respect to provision of contraception.Intrauterine device placement after delivery of the placenta is an appealing strategy for increasing access to postpartum Intrauterine device because it does not require a separate postpartum visit. Advantage of post-placental Intrauterine device insertion, Intrauterine devices are recommended as first-line contraceptives by the American Academy of Pediatricians. The Centers for Disease Control and Prevention united state . Medical Eligibility Criteria for Contraceptive Use places no restrictions on use, and states advantages generally outweigh the risks for immediate postpartum use of Intrauterine devices.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Intrauterine device insertion | Post-placental insertion of intrauterine device during Cesarean section |
| PROCEDURE | Cesarean section | to delivery of the fetus |
| PROCEDURE | Suture | to fix the intrauterine device |
Timeline
- Start date
- 2019-01-01
- Primary completion
- 2020-02-01
- Completion
- 2020-04-01
- First posted
- 2018-12-19
- Last updated
- 2021-09-16
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT03780985. Inclusion in this directory is not an endorsement.