Aortic Compression Trial to Reduce Blood Loss at Cesarean Section

Not Applicable

• Conditions: Post Partum Hemorrhage; Cesarean Section Complications; Anemia

• Registration Number: NCT05312658
• Lead Sponsor: Karolinska Institutet

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-3-28
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: Female
• Target Recruitment: 2232

Inclusion Criteria

Inclusion Criteria:<br><br> - Planned cesarean delivery<br><br> - Live fetus/fetuses if multiple pregnancy<br><br> - Gestational week 34+0 or more<br><br>Exclusion Criteria:<br><br> - Preoperative B-Hemoglobin <100 g/l<br><br> - Planned hysterectomy in the same procedure as the planned cesarean delivery<br><br> - Other condition as deemed by attending surgeon.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Calculated peripartum hemorrhage

Secondary Outcome Measures

Name	Time	Method
Peripartum hemorrhage (g);Hemoglobin and EVF change;Transfusion;Maternal death;Severe maternal morbidity;Duration of surgery;Duration of hospital stay