PostPlacental IUD Insertion

W

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)

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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