Comparative Effects of Focused and Unfocused (Radial) ESWT in the Treatment of Patellar Tendinopathy.

NCT ID: NCT05423366

Last Updated: 2023-02-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

75 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-16

Study Completion Date

2022-12-19

Brief Summary

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There is no scientific study in the literature regarding the use of different extracorporeal shock wave therapies (ESWT) in the treatment of patellar tendinopathy. In this study, we aim to investigate both the effectiveness of ESWT and which type of ESWT can be more effective in the treatment of patellar tendinopathy.

Detailed Description

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Conditions

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Patellar Tendinitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Large-Focused Extracorporeal Shock Wave Therapy

Group Type ACTIVE_COMPARATOR

Extracorporeal Shock Wave Therapy (ESWT)

Intervention Type DEVICE

The ESWT device is product of Elettronica Pagani, Italy.

Controlled-Unfocused (Radial) Extracorporeal Shock Wave Therapy

Group Type ACTIVE_COMPARATOR

Extracorporeal Shock Wave Therapy (ESWT)

Intervention Type DEVICE

The ESWT device is product of Elettronica Pagani, Italy.

Sham Extracorporeal Shock Wave Therapy

Group Type SHAM_COMPARATOR

Extracorporeal Shock Wave Therapy (ESWT)

Intervention Type DEVICE

The ESWT device is product of Elettronica Pagani, Italy.

Interventions

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Extracorporeal Shock Wave Therapy (ESWT)

The ESWT device is product of Elettronica Pagani, Italy.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Engaging in active sports, being 18 years or older, history of activity-related knee pain in the patellar tendon or patellar insertion, symptoms lasting longer than 8 weeks (non-acute), VISA-P score less than 80 before treatment, pain during knee loading on tendon or tendon it remains isolated in the limited part of the bone junction and does not spread to the entire patellar region (to differentiate patellar tendinopathy and patellofemoral pain).

Exclusion Criteria

* Being under the age of 18, acute knee or acute patellar tendon injury, chronic inflammatory joint diseases (rheumatoid arthritis, etc.), using immunosuppressive or corticosteroid medication in the last 6 months, previous knee surgery (in the anterior cruciate ligament or patellar tendon), knee in the last 1 month local (corticosteroid) injection, contraindications for ESWT treatment (eg pregnancy, malignancy, coagulopathy), previous ESWT treatment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yuzuncu Yıl University

OTHER

Sponsor Role lead

Responsible Party

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Volkan Şah

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Volkan Şah

Role: PRINCIPAL_INVESTIGATOR

Yüzüncü Yıl Üniversitesi Tıp Fakültesi

Locations

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Yuzuncu Yil University

Van, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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University of Van YüzüncüYıl

Identifier Type: -

Identifier Source: org_study_id

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