UnknownNot Applicable

Trans Caesarean Intra Uterine Contraceptive Device Insertion Versus Conventional Postpartum 6 Weeks Insertion

Egypt20 participantsStarted 2023-09-01

Plain-language summary

To compare immediate post-placental intrauterine contraceptive device insertion versus conventional placement at 6 weeks interval (often referred to as delayed or interval insertion) as regard to:- 1. Patient satisfaction. 2. Expulsion rate. 3. Complications

Who can participate

Age range18 Years – 40 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age: 18-40years. * Full term pregnancies delivered by cesarean section. * Desire to have intrauterine contraceptive device (Cu T) as a contraceptive option. * Agree to participate in the study. Exclusion Criteria: * Allergy to copper. * Ante- or intra-partum hemorrhage. * Ruptured of membranes for more than 18 h prior to delivery or Chorioamnionitis. * Known uterine abnormalities e.g., Bicornuate/septate Uterus, uterine myoma. * History of ectopic pregnancy. * Desire for pregnancy within 1 year of delivery. * Intrapartum fever \>38 c. * Sever thrombocytopenia.

What they're measuring

1-Patient satisfaction and complication.

Timeframe: 6 months

Trial details

NCT IDNCT06023849

SponsorAl-Azhar University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-08-30

Contact for this trial

Ahmed osman, M.B.B.Ch

01145883770 AhmedOsman.2244@azhar.edu.eg

View on ClinicalTrials.gov More IUD trials