Clinical Trials Logo

Clinical Trial Summary

To compare immediate post-placental intrauterine contraceptive device insertion versus conventional placement at 6 weeks interval (often referred to as delayed or interval insertion) as regard to:- 1. Patient satisfaction. 2. Expulsion rate. 3. Complications


Clinical Trial Description

Until the 1960s, Intrauterine devices (IUCDs) and condoms were the only artificial methods for the control of fertility. Nowadays ,despite the presence of 12 contraceptive methods which include 9 modern methods (pill, IUD, injectable, implant, vaginal methods (diaphragm and contraceptive foam or jelly), male condom, female sterilization, male sterilization, and emergency contraception) and 3 traditional methods (periodic abstinence, withdrawal, and prolonged breastfeeding , the insertion of an IUCD still the second most prevalent method of family planning used worldwide (13.6%), after female sterilization (20.5%), among women of reproductive age who are married or cohabiting. In Egypt, Egypt Demographic and Health Survey 2014 findings revealed that 59 percent of currently married women in Egypt are currently using a contraceptive method. The most widely used method is the IUD, followed by the pill and injectables. Thirty percent of currently married women are using the IUD, 16 percent are relying on the pill, and 9 percent are employing injectables. Relatively small proportions of women are using other modern methods, e.g., 1 percent reported currently using female sterilization. Two percent of women report use of traditional methods. There are two ways used in IUD insertion, in the postpartum period or immediate post-placental IUD insertion, in which the insertion of IUD occurs within ten minutes after placenta delivery and after the puerperium (after puerperal or interval period). Intrauterine device insertion during cesarean section was first introduced in 1967 by Zerzavy by suturing the IUD to the posterior uterine fundus. Research in China and Belgium introduced post-placental IUD insertion technique during cesarean delivery with placed an IUD as high as possible in the fundus without suturing the fundus wall. Intrauterine device insertion during early postpartum period is the most effective reversible contraceptive methods for many mothers because the contraception motivation is high, and it doesn't interfere with breast feeding. On the other hand, without an effective contraception in the first six weeks, woman may be accidentally pregnant. Hence, the mother prefers to insert IUD during cesarean delivery. As cesarean section (CS) rates are rising in all countries, IUD insertion at the time of CS creates an opportunity to increase access to long-acting reversible contraception methods. Conversely, a previous CS scar may deter access to interval insertion of an IUD if a previous CS may result in difficulty with insertion and/or future IUD problems. Inserting an IUD at the time of CS is a very attractive option; It adds very little time and cost to the procedure. The patient does not have to come back especially for follow-up, and there is no risk of primary perforation (secondary perforation is possible) as it is performed under direct vision. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06023849
Study type Interventional
Source Al-Azhar University
Contact Ahmed osman, M.B.B.Ch
Phone 01145883770
Email AhmedOsman.2244@azhar.edu.eg
Status Recruiting
Phase N/A
Start date September 1, 2023
Completion date September 2024

See also
  Status Clinical Trial Phase
Recruiting NCT03868137 - Multi-dose Ibuprofen Prophylaxis for IUD-insertion N/A
Completed NCT04539899 - Evaluation of the Influence of the Virtual Reality Helmet on Pain During IUD Insertion N/A
Completed NCT04932382 - Misoprostol Prior to Intrauterine Device Insertion N/A
Active, not recruiting NCT04927741 - Essential Oils Following IUD Insertion N/A
Completed NCT05383924 - Intrauterine Contraceptive Device Insertion During Cesarean Section (CS) Versus Delayed Insertion N/A
Completed NCT04389021 - Virtual Reality Simulation for Intrauterine Device Insertion: A Randomized Clinical Trial N/A
Completed NCT05187078 - Allis Clamp Versus Single-tooth Tenaculum N/A
Recruiting NCT05339555 - IUD Self-Removal Study N/A
Completed NCT04379102 - The Role Of Local Anesthetics in the Management of Adverse Effects Associated With Intrauterine Device Application
Recruiting NCT05875571 - Intravenous Ketorolac Administration to Attenuate Post-procedural Pain Associated With Intrauterine Device Placement Phase 4
Active, not recruiting NCT02076217 - Quick Start of Highly Effective Contraception
Recruiting NCT05700812 - IUD Placement Without Sounding N/A
Recruiting NCT05252117 - Uterovaginal Plexus Block With Articaine for Intrauterine Device Placement Patients Who Are Indicated for the Use of Copper IUD as a Contraceptive Method Will be Invited to Participate in This Research. Phase 4
Not yet recruiting NCT05471362 - Barriers of Immediate Postpartum Intrauterine Device Uptake
Not yet recruiting NCT04630548 - Safety and Efficacy of Immediate Post Placental IUD Insertion in Patients Undergoing Cesarean Delivery N/A
Not yet recruiting NCT05283798 - Insertion of Copper T380 Versus Multiload IUD Post Partum N/A
Not yet recruiting NCT06240260 - TENS Unit for Analgesia During IUD Insertion N/A
Completed NCT06042556 - IUD Self-Removal: Evaluating an Online Guide for Self-removal in Clinical and Non-clinical Settings N/A