← Back to all trials
Active Not Recruiting
NCT05624411
Clinical Outcomes of Post-placental Insertion of Cupper T380A and Multiload 375 Contraceptive Devices During Cesarean Section
Conditions: IUD (Intrauterine Device) Malposition, IUD; Complications, Infection or Inflammation
Sex: Female
Ages: 18 Years – 45 Years
Enrollment: 150
Sponsor: Sohag University
Location: Egypt
Summary
Clinical outcomes of post-placental insertion of Cupper T380A and Multiload 375 contraceptive devices during cesarean section
Eligibility Criteria
Inclusion Criteria:-(1) All patients admitted for delivery at our department who requested postpartum contraception, were invited to participate in the study.(2) Age (18-45)Exclusion Criteria:(1) Intrauterine infection at time of delivery (chorioamnionitis) (2) postpartum hemorrhage (3) Uterine anomalies (distorted uterine cavity) (4) History of previous IUD expulsion (5) Anemic patients with hemoglobin< 10gm/dl (6) pre-labor rupture of membranes for more than 18 hours (7) Placenta previa.
Source: ClinicalTrials.gov (NCT05624411). StuddyBuddy aggregates publicly available trial information.
