Evaluation of the effects of Foley ad Misoprostol association on the induction of labor

Not Applicable

• Conditions: ate pregnancy; G08.686.784.769

• Registration Number: RBR-7xcjz3z
• Lead Sponsor: niversidade Federal de Santa Catarina

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-02-15
• Study Completion: 2022-02-28
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Healthy volunteers; females; over 18 years old; pregnant women with 41 full weeks of gestation who require induction of labor; with Bishop's index less than 6.

Exclusion Criteria

Contraindication to the use of misoprostol. Contraindication to the use of Foley probe. Cervical dilation greater than or equal to 3 cm. Non-reassuring pre-induction cardiotocographic evaluation. Patients with high-risk pregnancies.

Study & Design

• Study Type: Intervention
• Study Design: Not specified