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RECRUITING
NCT07387380
NA

KIRA Uterine Drain Device Evaluation- First-In- Human Study

Sponsor: Lucie Medical Inc

View on ClinicalTrials.gov

Summary

The purpose of this research is to evaluate a new investigational medical device, the Kira device, intended to make it easier for the surgical team to monitor blood loss during and immediately after cesarean deliveries (c-sections). This study will assess the safety of the device and the device's ability to gently suction blood from the uterus into a clear container where it can be seen and measured by the surgical team.

Official title: KIRA Uterine Drain Device Evaluation - First-In- Human Study

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2026-01-06

Completion Date

2026-06

Last Updated

2026-02-04

Healthy Volunteers

No

Interventions

DEVICE

Uterine drain for use in cesarean section

The intervention will be used to remove uterine contents and measure blood loss immediately following cesarean delivery.

Locations (1)

Ohio State University

Columbus, Ohio, United States