CompletedNot Applicable

Intrauterine Contraceptive Device Insertion During Cesarean Section (CS) Versus Delayed Insertion

Egypt80 participantsStarted 2021-05-01

Plain-language summary

After ethical committee approval and written consent from the patients, this prospective quasi-randomized controlled clinical trial was performed on pregnant women planning to deliver by cesarean section and willing to participate in the study to investigate the value of immediate post placental IUD insertion versus delayed insertion on patient's compliance in Ain Shams University Maternity Hospital (ASUMH).

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: * Pregnant women planned for delivery by cesarean section in Ain Shams University Maternity hospital Exclusion Criteria: * Women not consenting to use IUD as a contraceptive method and preferring other methods. * Any woman with condition included in Category 3 or 4 for Cu-IUD in medical eligibility criteria for contraceptive use World Health Organization (WHO) 2015 * Neuropsychiatric disorder causing altered mentality or perception * Intrapartum complications as chorioamnionitis, massive blood loss, or hysterectomy. * Anemic patients (hemoglobin level \<10g/dl).

What they're measuring

Patient compliance

Timeframe: at 6 months after the procedure

Patient compliance

Timeframe: at 12 months after the procedure

Trial details

NCT IDNCT05383924

SponsorAin Shams Maternity Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-05-01

View on ClinicalTrials.gov More Contraception trials