Post-Market Evaluation of the Rotation Medical Rotator Cuff System

NACompletedINTERVENTIONAL
Enrollment

148

Participants

Timeline

Start Date

August 20, 2014

Primary Completion Date

November 24, 2020

Study Completion Date

November 24, 2020

Conditions
Partial Thickness Supraspinatus Tendon TearFull Thickness Supraspinatus Tendon Tear
Interventions
DEVICE

Bioinductive implant

DEVICE

Surgical repair

Surgical repair with commercially-available sutures/suture anchors.

Trial Locations (15)

21204

Towson Orthopaedic Associates / University of Maryland St Joseph Med Ctr, Towson

28207

OrthoCarolina Research Institute, Charlotte

30165

Harbin Clinic Orthopaedics & Sports Medicine Rome, Rome

33334

Holy Cross Hospital Orthopedic Research Institute, Fort Lauderdale

44125

Cleveland Clinic, Cleveland

49684

Great Lakes Orthopaedic Center, Traverse City

52242

University of Iowa Sports Medicine, Iowa City

55435

Twin Cities Orthopedics, Edina

61107

OrthoIllinois, LTD, Rockford

76021

Texas Orthopedic Specialists, P.L.L.C., Bedford

77030

Bone & Joint Clinic of Houston, Houston

80111

Steadman Hawkins Clinic-Denver, Denver

91405

Southern California Orthopedic Institute, Van Nuys

98034

ProOrtho Orthopedic Clinic, Kirkland

08540

Princeton Orthopaedic Associates, P.A., Princeton

All Listed Sponsors
lead

Smith & Nephew, Inc.

INDUSTRY

NCT02200939 - Post-Market Evaluation of the Rotation Medical Rotator Cuff System | Biotech Hunter | Biotech Hunter