DAISY Uterine Drain Device Evaluation
NCT: NCT06219538 · COMPLETED
Brief 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.
Frequently Asked Questions
What is DAISY Uterine Drain Device Evaluation?
DAISY Uterine Drain Device Evaluation is a clinical trial registered under NCT06219538. Current status: COMPLETED.
What is the status of NCT06219538?
The current status of NCT06219538 (DAISY Uterine Drain Device Evaluation) is: COMPLETED.
When did DAISY Uterine Drain Device Evaluation start?
DAISY Uterine Drain Device Evaluation started on 2024-05-22.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.