Skip to main content
Clinical Trials/NCT05148416
NCT05148416CompletedNot Applicable

Effect of High Intensity Laser in Treatment of Myofascial Trigger Points in Symptomatic Knee Osteoarthritis : A Randomized Single-blinded Controlled Trial

Cairo University1 site in 1 country40 target enrollmentStarted: February 1, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Pain Intensity: change of serum cortisol level was used in many research as pain blood biomarker

Study Overview

Brief Summary

This study was conducted to investigate the effect of High intensity laser therapy( HILT) on pressure pain threshold, serum cortisol level, passive knee range of motion, and changes of functional disability in patients with active myofascial trigger points(MTrPs) pain associated wit knee osteoarthritis(OA) .

Detailed Description

Osteoarthritis (OA) is the most common cause of musculoskeletal pain and disability. It is a chronic degenerative disorder of multifactorial etiology, including acute and/or chronic insults from normal wear and tear, age, obesity and joint injury. The true pathogenesis remains poorly understood. OA is characterized by a degradation of the articular cartilage, resulting in an alteration of its biomechanical properties, which in turn contributes to a focal loss of articular cartilage, loss of joint space, osteophyte formation, focal areas of synovitis, per articular bone remodeling and sub chondral cysts , OA presents with symptoms such as joint pain, stiffness, motion limitations, motor and sensory dysfunction and functional impairments, thus, preventing patients from participating in regular physical activities , The common sites of OA appear on the knees, hands, and hips, whereas knee OA is the most common .

Pain is the most frequent complaint for patients with knee OA to seek medical attention. If left untreated, pain and stiffness can result in a loss of physical function and independence during daily activities. The presence of OA-related knee pain has also been associated with increased risks of physical disability in the community .

Many studies have revealed a discrepancy between patients' reports of pain and their radiographic findings , a plausible option is that the pain originates from the myofascial trigger points (MTrPs) in the surrounding muscles (myofascial pain) and cannot be visualized by imaging.

The term myofascial pain is defined as "the complex of sensory, motor, and autonomic symptoms caused by MTrPs , MTrPs, hyperirritable spots found in the skeletal muscles, are associated with hypersensitive palpable nodules located in a taut band. The spots are painful on compression and may produce characteristic referred pain, referred tenderness, motor dysfunction, and autonomic phenomena.

All studies found a high prevalence of myofascial pain in knee OA patients . study of OA patients, MTrPs were found in all participants, especially in the medial head of the gastrocnemius (92%) and the vastus medialis muscle (67%).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
35 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients diagnosed as II degree bilateral knee OA having active MTrP in vastus medialis and medial head of gastrocnemius muscles and over the calf muscle .
  • The patients from both gender aged were ranged from 35 to 55 years.

Exclusion Criteria

  • Reactive synovitis, corticosteroids or hyaluronic acid application during the last six months
  • Not indicated and no history of knee joint arthroplastic surgery.
  • Malignant tumors and chronic infection.
  • Not diagnosed with cushing's syndrome.

Arms & Interventions

Laser group

Experimental
  1. Experimental group (A) the laser group (n=20) which received

  2. high intensity laser therapy(HILT)

  3. knee osteoarthritis conventional exercises program in form of stretching exercises for both vastus medialis and gastrocnemius muscles , ROM exercises for knee flexion and extension , and isometric strengthening exercise of previously mentioned muscles .

all interventions were done under the supervision of physiotherapist for 30 minutes once a day for 3 days per week during a period of 4 weeks.

Intervention: High intensity laser treatment (Radiation)

Laser group

Experimental
  1. Experimental group (A) the laser group (n=20) which received

  2. high intensity laser therapy(HILT)

  3. knee osteoarthritis conventional exercises program in form of stretching exercises for both vastus medialis and gastrocnemius muscles , ROM exercises for knee flexion and extension , and isometric strengthening exercise of previously mentioned muscles .

all interventions were done under the supervision of physiotherapist for 30 minutes once a day for 3 days per week during a period of 4 weeks.

Intervention: knee osteoarthritis conventional exercises program (Other)

the sham group group( B)

Sham Comparator

the Sham group (n= 20) which received

  1. sham HILT
  2. knee osteoarthritis conventional exercises program previously mentioned .

all interventions were done under the supervision of physiotherapist for 30 minutes once a day for 3 days per week during a period of 4 weeks.

Intervention: sham HILT. (Device)

the sham group group( B)

Sham Comparator

the Sham group (n= 20) which received

  1. sham HILT
  2. knee osteoarthritis conventional exercises program previously mentioned .

all interventions were done under the supervision of physiotherapist for 30 minutes once a day for 3 days per week during a period of 4 weeks.

Intervention: knee osteoarthritis conventional exercises program (Other)

Outcomes

Primary Outcomes

Pain Intensity: change of serum cortisol level was used in many research as pain blood biomarker

Time Frame: The first sample was obtained before the first day of treatment and the second sample was obtained after 4 weeks (1 month) of treatment

For measuring serum cortisol level, Each patient was drawn two 5 ml blood samples from cubital vein two times.

Secondary Outcomes

  • Pressure pain threshold: The Commander Algometer (JTECH Medical, Midvale, Utah, USA) was used to measure the PPT.(The first measure was obtained before the first day's treatment and the second measure was obtained after 4 weeks of treatment (1 month).)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Bassant Basiony Ahmed Basiony

physiotherapist

Cairo University

Study Sites (1)

Loading locations...

Similar Trials