Insertion of a copper IUD after immediate vaginal delivery: comparison between placement with and without the aid of ultrasound

Not Applicable

Recruiting

• Conditions: Family Development Planning; SP2.770.875

• Registration Number: RBR-10mn89c6
• Lead Sponsor: Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2024-02-16
• Last Update Posted: 5 March 2024
• Study Completion: 2027-12-31

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Pregnant women with a single fetus. Age over 18 years old. Gestational age greater than or equal to 34 weeks. Pregnant women admitted to an obstetric center in early labor (< 4 cm cervical dilation) or under labor analgesia, able to understand the study presentation, its justification and sign the informed consent form. Pregnant women expressing a desire to insert an IUD prior to the study inclusion interview

Exclusion Criteria

Puerperal sepsis. Chorioamnionitis. Distorted uterine cavity (submucous myoma, Mullerian malformations). Cervical cancer. Fever (oral temperature = 37.8º C) during labor. Rupture of ovular membranes = 18 hours. Puerperal hemorrhage when any type of intervention is performed for puerperal hemorrhage: Manual massage, Administration of crystalloid for volume expansion or blood derivatives. Use of medications such as oxytocin, ergotamine, misoprostol, tranexamic acid. Use of intrauterine balloon. Surgical treatment such as vessel ligation and B-Lynch.

Study & Design

• Study Type: Intervention
• Study Design: Not specified