Actively Recruiting

Age: 18Years - 60Years
All Genders
Healthy Volunteers
ID07314840

Ultrasonographic Examination of Other Enthesitis Sites in Patients With Lateral Epicondylitis: A Cross-Sectional Study

Led by Marmara University · Updated on 2026-01-02

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to investigate the relationship between genetic factors linked to tendinopathies and lateral epicondylitis (LE), which is a condition involving tendinopathy of the common extensor tendon believed to be caused by overuse. The study will assess the use of the Madrid Sonographic Enthesitis Index (MASEI), an ultrasound scoring system originally developed for ankylosing spondylitis but now applied to other musculoskeletal diseases, to evaluate enthesitis in patients with LE compared to healthy individuals. Participants will be grouped into two: those diagnosed with lateral epicondylitis and healthy volunteers with similar demographic characteristics. The MASEI evaluation involves ultrasound scans at 12 specific tendon insertion sites including the triceps brachii, quadriceps, patellar tendons, Achilles tendon, and plantar fascia. The ultrasound examines tendon structure and thickness, calcifications, erosions, bursitis, and power-Doppler signals at these sites. During the study, participants will undergo ultrasound examinations to obtain MASEI scores at enrollment. Researchers will compare these scores between the LE patients and healthy volunteers to understand enthesitis involvement. The study expects to monitor these ultrasound findings as the primary outcome measure and will last until January 2026, involving adults aged 18 to 60 years.

CONDITIONS

Brief Title

Ultrasonographic Examination of Other Enthesitis Sites in Patients With Lateral Epicondylitis

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Tenderness with palpation at the lateral epicondyle
  • Pain aggravated with resisted wrist extension
  • Adults aged 18 to 60 years
Not Eligible

You will not qualify if you...

  • History of rheumatologic diseases
  • History of elbow, knee or ankle surgery
  • History of corticosteroid injections on elbow, knee or ankle
  • History of peripheral neuropathy
  • Acute trauma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - At enrollment

Participants undergo ultrasound evaluation at multiple tendon insertion sites to assess tendon structure, thickness, and presence of abnormalities.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Marmara University

Istanbul, Maltepe, Turkey (Türkiye), 34844

Actively Recruiting

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Research Team

A

Arda Can Kasap, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

Ultrasonographic Evaluation of Lower Extremity Entheseal Sites in Diabetic Patients Using Glasgow Ultrasound Enthesitis Scoring System Score.

Sibel Caglar Okur, Yasemin Pekin Dogan, Murat Mert...

https://pubmed.ncbi.nlm.nih.gov/30065480

Diagnostic accuracy of examination tests for lateral elbow tendinopathy (LET) - A systematic review.

Stefanos Karanasios, Vasileios Korakakis, Maria Moutzouri...

https://pubmed.ncbi.nlm.nih.gov/33814224