Clinical Trials Directory

Trials / Completed

CompletedNCT01235715

The Use of Evicel to Reduce Blood Loss in Total Knee Replacement Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Hospital for Special Surgery, New York · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Application of "Evicel" hemostatic matrix during operation for unilateral total knee replacement surgery (TKA) will result in decreased bleeding and postoperative drain output, a reduction in transfusion requirements, and less reduction of hemoglobin.

Detailed description

No additional data desired

Conditions

Interventions

TypeNameDescription
DRUGEvicel fibrin sealantUsed for hemostasis to control bleeding. It has been shown to stop bleeding in 2 minutes or less. It is a combination of a biologic activated component containing human fibrinogen and topical thrombin functioning on wet, actively bleeding tissue.

Timeline

Start date
2010-09-01
Primary completion
2012-03-01
Completion
2012-09-01
First posted
2010-11-05
Last updated
2013-10-29
Results posted
2013-10-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01235715. Inclusion in this directory is not an endorsement.