PostPlacental IUD Insertion

Woman's Health University Hospital, Egypt

Status: Completed

Conditions: Contraception

Treatments: Device: Copper T intrauterine device

Study type: Interventional

Funder types: Other

Identifiers

NCT02679820

LA010516

Details and patient eligibility

About

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

Enrollment: 500 patients

Sex: Female

Ages: 20 to 45 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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500 participants in 2 patient groups

PostPlacental IUD insertion

Experimental group

Description:

Copper T intrauterine device will be inserted immediately following delivery of the placenta in cases of cesarean section deliveries.

Treatment:

Device: Copper T intrauterine device

Control

No Intervention group

Description:

IUD will be offered as a method of contraception after puerperium