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Study identifier: NCT05545930 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Blood Recovery  ·  Sponsor: University Hospitals Cleveland Medical Center

PhaseNA
Planned participants20
Who can joinAll sexes, 18 Years to 89 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Jessica Hungate, MD  ·  216-844-3800  ·  Jessica.Hungate@UHhospitals.org

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospitals Cleveland Medical CenterCleveland, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05545930