NCT05545956

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

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: University Hospitals Cleveland Medical Center · Academic / Other
• Sex: All
• Age: 18 Years – 89 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Blood Recovery

Interventions

Type	Name	Description
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).

Timeline

• Start date: 2023-05-09
• Primary completion: 2025-01-01
• Completion: 2025-01-01
• First posted: 2022-09-19
• Last updated: 2024-12-24

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study