To evaluate the acute and long-term clinical outcomes of tenotomy with the TenJet System in patients with elbow tendinosis.
This is a prospective, non-randomized, single arm post-marketing clinical study of patients undergoing percutaneous ultrasound guided medial and lateral tenotomy using the TenJet HydroSurgery System to treat elbow tendinosis. Patients will be followed for a maximum of 12 months post-procedure.
Study Type
OBSERVATIONAL
Enrollment
29
Percutaneous ultrasound guided medial and lateral tenotomy using the TenJet HydroSurgery System
Orthopaedic Associates of Muskegon
Muskegon, Michigan, United States
Penn Highlands
DuBois, Pennsylvania, United States
Noble Pain Management & Sports Medicine
Fort Worth, Texas, United States
Change in Elbow Pain Using Visual Analog Scale (VAS)
Change in elbow pain (VAS) compared with baseline. VAS range 0 (no pain) to 10 (intolerable pain); higher scores indicate worse pain. Mean change is calculated as baseline minus follow-up, so positive values indicate improvement. Time points: 2 weeks, 6 weeks, 3 months, 6 months, 12 months.
Time frame: Up to 12 months
Change in Elbow Function Using the Patient-Rated Elbow Evaluation Questionnaire (PREE)
Change in total PREE score compared with baseline on a 0-100 scale (lower scores indicate less pain/higher function). Mean change is calculated as baseline minus follow-up (positive = improvement) and reported at 2 weeks, 6 weeks, 3 months, 6 months, and 12 months.
Time frame: Up to 12 months
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