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

University Hospitals (UH) logo

University Hospitals (UH)

Status

Withdrawn

Conditions

Blood Recovery

Treatments

Procedure: Hand Wrung
Device: ProCell Wrung

Study type

Interventional

Funder types

Other

Identifiers

NCT05545956
STUDY20220888_2

Details and patient eligibility

About

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.

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Undergoing heart or lung transplant, redo sternotomy, aortic surgery, and/or multi-valve repairs/replacements; and
  • At University Hospitals Cleveland Medical Center.

Exclusion criteria

  • Patients with known bleeding disorders, including disseminated intravascular coagulation (DIC), prothrombin deficiency, factor V deficiency, factor VII deficiency, factor X deficiency, factor XI deficiency (hemophilia C), Glanzmann disease, hemophilia A, hemophilia B, idiopathic thrombocytopenic purpura (ITP), and Von Willebrand disease (types I, II, and III);
  • Patients undergoing emergent or emergent salvage surgery; and
  • Patients actively participating in another clinical trial which could affect outcomes.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Hand Wrung
Active Comparator group
Description:
Hand wrung refers to manually wringing surgical sponges by hand.
Treatment:
Procedure: Hand Wrung
ProCell Wrung
Experimental group
Description:
ProCell wrung refers to automated wringing surgical sponges by an FDA approved suction device (ProCell).
Treatment:
Device: ProCell Wrung

Trial contacts and locations

1

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Central trial contact

Craig Jarrett, MD, MBA

Data sourced from clinicaltrials.gov

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