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OpenTrials
Completed

NCT Number: NCT03780985

Post-placental Intrauterine Device Insertion During Cesarean Section

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.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Woman's Health Hospital - Assiut university

Asyut, 71111, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age group : 18-40 years
  • Women who will be willing to undergo elective cesarean section
  • women desire using Copper IUD as long acting contraceptive method.

Exclusion criteria

  • Intrauterine infection.
  • Fundal Myoma.
  • Hemorrhagic disorder
  • Genital tract malignancy
  • Uterine atony
  • Sexually transmitted infection.

Treatment and study plan

Intrauterine device insertion

Procedure

Post-placental insertion of intrauterine device during Cesarean section

cesarean section

Procedure

to delivery of the fetus

Suture

Procedure

to fix the intrauterine device

Primary outcomes

  1. Number of displaced intrauterine device after insertion in both groups

    Time frame: 2 weeks

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Hang-up Versus Non-fixation Technique for Immediate Post-placental Intrauterine Device Insertion During Cesarean Section

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Dec 19, 2018
Registry last updated
Sep 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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