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LEICeSter Tendon Extracorporeal Shockwave Studies

NCT02546128 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 720

Last updated 2024-05-01

No results posted yet for this study

Summary

To assess whether the addition of Extra-corporeal Shockwave Therapy (ESWT) to a structured home-exercise programme has any additional benefit to patients with tendinopathies

Conditions

  • Tendinopathy

Interventions

DEVICE

Extra-Corporeal Shockwave Therapy (ESWT)

The use of ESWT from a commercially available machine at approved settings already in routine clinical use

OTHER

structured rehabilitation programme

a structured and standardised rehabilitation programme specific to the tendon in question - already in routine clinical use

Sponsors & Collaborators

  • University Hospitals, Leicester

    lead OTHER

Principal Investigators

  • Patrick Wheeler · UHL NHS Trust

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • United Kingdom

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 NCT02546128 on ClinicalTrials.gov