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DAISY Uterine Drain Device Evaluation
Sponsor: Raydiant Oximetry, Inc.
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
Conditions
Interventions
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