findmyKOL
Clinical trialNCT06452355Active, not recruitingInterventional

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

SponsorKOKO Medical Inc.Enrollment72Hemorrhage, PostpartumImmediate Postpartum HemorrhagePostpartum Hemorrhage
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

17 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of Alabama

    Birmingham, Alabama, United States

  • Christiana Care

    Newark, Delaware, United States

  • University of Miami

    Miami, Florida, United States

  • Indiana University School of Medicine, Dept. of Obgyn

    Indianapolis, Indiana, United States

  • University of Kentucky

    Lexington, Kentucky, United States

  • Lsu Heath Sciences Center - Shreveport

    Shreveport, Louisiana, United States

  • Sunrise Hospital and Medical Center

    Las Vegas, Nevada, United States

  • New York-Presbyterian Medical Group Queens

    Flushing, New York, United States

  • New York-Presbyterian Hospital (nyph)/columbia University Irving Medical Center (cuimc)

    New York, New York, United States

  • Duke University

    Durham, North Carolina, United States

  • Metrohealth

    Cleveland, Ohio, United States

  • the Cleveland Clinic

    Cleveland, Ohio, United States

  • the Ohio State University

    Columbus, Ohio, United States

  • Medical University of South Carolina

    Charleston, South Carolina, United States

  • Baylor College of Medicine

    Houston, Texas, United States

  • Ut Health Houston

    Houston, Texas, United States

  • University of Utah

    Salt Lake City, Utah, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
29 Aug 2024
Primary completion
30 Aug 2026
Completion
30 Sept 2026
Last update posted
2 Jul 2026
Registered enrollment
72
Registry id
NCT06452355

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.