PostPlacental IUD Insertion

Not Applicable

Completed

• Conditions: Contraception
• Interventions: Device: Copper T intrauterine device

• Registration Number: NCT02679820
• Lead Sponsor: Woman's Health University Hospital, Egypt

Brief Summary

The immediate post cesarean section IUD insertion is a further step towards spreading more compliance to females in developing countries, with rapid increase in population size

Detailed Description

Not available

Study Timeline

• Study Start: 2016-01
• Study First Submitted: 2016-02-08
• Study First Submitted QC: 2016-02-08
• Study First Posted: 2016-02-10
• Primary Completion: 2018-12
• Study Completion: 2018-12
• Status Verified: 2019-01
• Last Update Submitted: 2019-01-06
• Last Update Posted: 2019-01-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 500

Inclusion Criteria

• Females desiring contraception by using intrauterine device following their vaginal delivery or cesarean section

Exclusion Criteria

• refusal to participate in the study
• desiring other methods of contraception
• will not use any method of contraception
• has a contraindication for the use of IUD as bicornuate or septate uterus, sub mucous myomas, etc.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
PostPlacental IUD insertion	Copper T intrauterine device	Copper T intrauterine device will be inserted immediately following delivery of the placenta in cases of cesarean section deliveries.

Primary Outcome Measures

Name	Time	Method
The percentage of females seeking contraception	6 months
Expulsion rate	6 months

Trial Locations

Locations (1)

Kasr el aini hospital; 🇪🇬 Cairo, Egypt