Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06965985

Comparison of the Effectiveness of Mulligan Mobilization and Myofascial Release Technique in Patients With Lateral Epicondylitis

Led by Konya Beyhekim Training and Research Hospital · Updated on 2025-05-11

114

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Lateral epicondylitis (LE), recognized as one of the most prevalent causes of elbow pain, has an estimated incidence ranging from 1% to 3%. It most commonly presents in individuals between the ages of 40 and 50 and tends to affect the dominant limb more frequently. In the adult population, LE is the leading cause of lateral elbow pain. To date, more than 40 different treatment modalities have been described for the management of LE, primarily aiming to alleviate pain and enhance functional outcomes. However, a universally accepted standard treatment has yet to be established. The objective of this thesis is to compare the clinical effectiveness of the Mulligan mobilization technique and the myofascial release technique-both commonly utilized in the treatment of LE-through a prospective clinical study.

CONDITIONS

Official Title

Comparison of the Effectiveness of Mulligan Mobilization and Myofascial Release Technique in Patients With Lateral Epicondylitis

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged between 18 and 65 years
  • Diagnosed with unilateral lateral epicondylitis (LE)
Not Eligible

You will not qualify if you...

  • Younger than 18 or older than 65 years
  • Communication difficulties
  • History of injection, surgery, or physical therapy in the elbow region within the past 6 months
  • Pain from cervical spine issues, shoulder problems, or other elbow conditions not related to LE
  • History of elbow osteoarthritis or previous elbow fracture
  • History of polyneuropathy
  • Uncontrolled systemic diseases such as cardiovascular, pulmonary, hepatic, renal, or hematologic disorders
  • Uncontrolled systemic endocrine disorders such as diabetes mellitus or hyperthyroidism
  • History of major psychiatric disorders
  • History of rheumatic diseases including fibromyalgia, polymyalgia rheumatica, ankylosing spondylitis, or rheumatoid arthritis
  • Presence of bleeding disorders or use of anticoagulant medications
  • Neurological deficits
  • Posterior interosseous nerve (PIN) syndrome
  • Current or past use of wrist resting splints or elbow braces

AI-Screening

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Trial Site Locations

Total: 1 location

1

Konya Beyhekim Eğitim ve Araştırma Hastanesi

Konya, Selçuklu, Turkey (Türkiye), 42060

Actively Recruiting

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Research Team

C

Cansu Ertuğrul

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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