Total Knee Arthroplasty Clinical Trial
Official title:
Retrospective & Prospective Evaluation/Analysis of Hb/Hct in Patients Having Received FloSeal (5ml &10ml) When Undergoing Total Knee or Total Hip Arthroplasty
The purpose of this analysis is to compare Hemoglobin and Hematocrit levels following total hip or knee arthroplasty. The utilization of FloSeal intraoperatively will improve hemostasis postoperatively. Decreasing bleeding time will decrease the drop in level of Hemoglobin and Hematocrit which usually occurs postoperatively.
Status | Not yet recruiting |
Enrollment | 500 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 95 Years |
Eligibility |
Inclusion Criteria: - Total Knee and Total Hip Patients - Surgical Time less than 2 hours Exclusion Criteria: - Patients who require greater than 2 hour surgeries - Patients who are undergoing revision arthroplasty - Patients with known allergies to materials of bovine origin |
Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
United States | Desert Orthopedic Center | Rancho Mirage | California |
Lead Sponsor | Collaborator |
---|---|
Desert Orthopedic Center Medical Research Foundation | Baxter Healthcare Corporation |
United States,
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