CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 10 enrolled
Drug / intervention
DAISY Uterine Draindevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06219538
NCT06219538N/ACompleted

DAISY Uterine Drain: Device Evaluation With Standard Wall Suction

Raydiant Oximetry, Inc.·interventional·Posted Jan 23, 2024·Updated May 1, 2026

In Brief

A clinical study evaluating DAISY Uterine Drain for Cesarean Section Complications and 3 related conditions. Completed, enrolled 10 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202420252026
First PostedJan 23, 2024
Enrollment StartMay 22, 2024
Primary CompletionApr 16, 2025
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 2.4 years ago

Interventions

DAISY Uterine Draindevice

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