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Clinical Trials/NCT02679820
NCT02679820
Completed
Not Applicable

PostPlacental IUD Insertion

Woman's Health University Hospital, Egypt1 site in 1 country500 target enrollmentJanuary 2016
ConditionsContraception

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraception
Sponsor
Woman's Health University Hospital, Egypt
Enrollment
500
Locations
1
Primary Endpoint
The percentage of females seeking contraception
Status
Completed
Last Updated
7 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
December 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Woman's Health University Hospital, Egypt
Responsible Party
Principal Investigator
Principal Investigator

Dina Mohamed Refaat Dakhly

Lecturer of Obstetrics and Gynecology

Woman's Health University Hospital, Egypt

Eligibility Criteria

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.

Outcomes

Primary Outcomes

The percentage of females seeking contraception

Time Frame: 6 months

Expulsion rate

Time Frame: 6 months

Study Sites (1)

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