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Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System

NCT03487250 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 29

Last updated 2026-05-07

Study results available
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Summary

To evaluate the acute and long-term clinical outcomes of tenotomy with the TenJet System in patients with elbow tendinosis.

Conditions

  • Elbow, Tennis

Interventions

DEVICE

TenJet System

Percutaneous ultrasound guided medial and lateral tenotomy using the TenJet HydroSurgery System

Sponsors & Collaborators

  • HydroCision, Inc.

    lead INDUSTRY

Principal Investigators

  • Reginald Kapteyn, DO · Orthopaedic Associates of Muskegon

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-04
Primary Completion
2019-04-20
Completion
2019-04-20
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03487250 on ClinicalTrials.gov