Vascular Changes of Rotator Cuff Repair Augmented With a Whole Blood Fibrin Clot

NACompletedINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

March 1, 2019

Primary Completion Date

April 25, 2022

Study Completion Date

April 25, 2022

Conditions
Rotator Cuff Tear
Interventions
OTHER

Whole Blood Fibrin Clot

For all patients assigned to the treatment group, 35mL of whole blood will be obtained during surgery by an anesthesiologist. 5 mL of the blood will be sent for pre-clot formation cell count evaluation for platelets, red blood cells and white blood cells. The remaining 30mL will be placed into a sterile container with a sintered glass cylinder supported by the lid for fibrin clot formation. The clot formation cups will be placed on a rotator at room temperature for 10 minutes at 125rpm. The fibrin clot will be removed and 5mL of the post-clot serum sent for post-clot formation cell count evaluation for platelets, red blood cells, and white blood cells.

Trial Locations (1)

93101

De La Vina Surgery Center, Santa Barbara

All Listed Sponsors
lead

Santa Barbara Cottage Hospital

OTHER

NCT03577379 - Vascular Changes of Rotator Cuff Repair Augmented With a Whole Blood Fibrin Clot | Biotech Hunter | Biotech Hunter