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COMPLETED
NCT06219538
NA

DAISY Uterine Drain Device Evaluation

Sponsor: Raydiant Oximetry, Inc.

View on ClinicalTrials.gov

Summary

The goal of this study is to obtain user feedback while placing and observing the DAISY uterine drain with wall suction. This study defines the obstetrical surgeons as "users" and the patients in whom the drain is placed as "participants." Participants are pregnant women who are undergoing cesarean delivery (CD), who have not entered active labor, who have consented to drain placement and who have met all the inclusion/exclusion criteria. Users are staff or fellow obstetrical surgeons who will use the drain and provide the evaluation.

Official title: DAISY Uterine Drain: Device Evaluation With Standard Wall Suction

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2024-05-22

Completion Date

2025-04-16

Last Updated

2026-05-01

Healthy Volunteers

Yes

Interventions

DEVICE

DAISY Uterine Drain

Insertion of the DAISY Uterine Drain and connection to wall suction in women who have undergone a Caesarean Delivery,

Locations (1)

Eastern Virginia Medical School

Norfolk, Virginia, United States