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RECRUITING
NCT05545930
NA

Analysis of Red Blood Cell Integrity and Efficiency of Recovery Using a Novel Surgical Sponge-Blood Recovery Device (ProCell)

Sponsor: University Hospitals Cleveland Medical Center

View on ClinicalTrials.gov

Summary

The purpose of this research study is to compare two methods of recovering blood from surgical sponges used during heart and lung surgeries. The two methods are: 1) manually wringing sponges by hand, and 2) automated wringing sponges by an FDA approved suction device. Both methods are already in use in heart and lung surgeries at University Hospitals at the discretion of the surgeon.

Key Details

Gender

All

Age Range

18 Years - 89 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2022-09-20

Completion Date

2026-07-01

Last Updated

2026-01-07

Healthy Volunteers

No

Conditions

Interventions

PROCEDURE

Hand Wrung

Hand wrung refers to manually wringing surgical sponges by hand.

DEVICE

ProCell Wrung

ProCell wrung refers to automated wringing surgical sponges by an FDA approved suction device (ProCell).

Locations (1)

University Hospitals Cleveland Medical Center

Cleveland, Ohio, United States