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Clinical Trial Summary

The ACCEL® Absorbable Hemostat Powder Clinical IDE Trial is designed as a prospective, multi-center, randomized, non-inferiority, controlled pivotal clinical trial to evaluate the safety and efficacy of the ACCEL® Absorbable Hemostat Powder as compared to gelatin sponge, for achieving hemostasis in subjects undergoing cardiovascular, liver, or soft tissue surgery, when control of oozing to moderate bleeding by standard surgical techniques is ineffective and/or impractical.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04728087
Study type Interventional
Source Hemostasis, LLC
Contact Aurelius D Butler, MS
Phone 651-621-8295
Email AButler@hemostasisllc.com
Status Recruiting
Phase N/A
Start date October 26, 2021
Completion date June 30, 2024

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