CompletedInterventionalNot ApplicableUpdated Jan 9, 2019
PostPlacental IUD Insertion
ClinicalTrials.gov ID
NCT02679820
Lead Sponsor
Woman's Health University Hospital, EgyptOTHER
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
500Actual
Last Update Posted
Jan 9, 2019Actual
Start Date
Jan 2016
Primary Completion Date
Dec 2018Actual
Completion Date
Dec 2018Actual
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
Contraception
Copper T intrauterine device
Ages Eligible for Study
Adult (18-64)
Sexes Eligible for Study
Female
Accepts Healthy Volunteers
Yes
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.