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Safety and Effectiveness of the KOKO Device to Treat Primary Abnormal Postpartum Uterine Bleeding or Hemorrhage — SERENE  

Postpartum Hemorrhage Clinical Trial

Official title:
Clinical Trial Designed to Assess the Safety and Effectiveness of the KOKO™ Device In Treating Primary Abnormal Postpartum Uterine Bleeding ("APUB") or Hemorrhage ("PPH")

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of the KOKO™ device in the control and reduction of primary abnormal postpartum uterine bleeding or hemorrhage.

Clinical Trial Description

This IDE study is designed to evaluate the effectiveness and safety of the KOKO™ device to treat primary abnormal postpartum uterine bleeding or hemorrhage. The study is literature controlled. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06452355
Study type Interventional
Source KOKO Medical Inc.
Contact Cathy Unruh
Phone 610-215-2011
Email cathyu@kokomed.com
Status Not yet recruiting
Phase N/A
Start date June 30, 2024
Completion date July 30, 2025
View Details
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