High-intensity Laser Therapy Versus Extracorporeal Shock Wave on Tendon Thickness and Occupation Ratio In Patients With Chronic Supraspinatus Tendinopathy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorCairo University

About this trial

This study will be conducted to investigate the difference between high-intensity laser and extracorporeal shock wave on supraspinatus tendon thickness, subacromial space, occupation ratio, shoulder pain intensity, shoulder range of motion (ROM), hand strength, and functional disability in patients with chronic supraspinatus tendinopathy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients from 18 to 50 years old of both genders.

Unilateral Chronic Supraspinatus Tendinitis in dominant side

BMI 18.5-24.9

Tenderness is found over the supraspinatus as it passes subacromial and anterolateral The patient will report pain with active shoulder elevation in the scapular plane (eg: welders, plate workers, slaughterhouse workers and overhead playing athletes)

Disqualifiers

Post shoulder surgery, traumatic incidents

Partial tears at surgery

Massive retracted tears at surgery

Frozen shoulder Rotator cuff tear

Trial design

Design model

Parallel

Treatments tested in this trial

  • High-intensity Laser Therapy

    Other intervention

    the patients will receive HILT with peak power 3kW, intensity 15000W/cm and energy per pulse 350 mj) at supraspinatus tendenopathy.The treatment consisted of 3 phases in each session. the initial phase will be rapid manual scanning (100 cm2/30s) of the anterior joint line of the shoulder with one shot of 850 mj at frequency of 30 Hz. The scanning will be performed parallel to the joint line, with the patient arm internally rotated on the posterior scan and externally rotated on the anterior scan. the intermediate phase will be a fixed scan phase , with one -shot emission of 350mj at a frequency of 20-25Hz. plus conventional therapy

  • Extracorporeal Shock Wave

    Other intervention

    patients will be sitting with shoulder abduction at 45 and elbow flexed and the forearm rested on flat surface and shock wave applicator directed in the most tender point near the insertion at the greater tubrosity under acromion with 2000 impulses, and energy flex density of 0.22mj/mm , pulse rate 10/sec and frequency 1-15 Hz plus conventional therapy

  • conventional therapy

    Other intervention

    will receive Conventional physical therapy in form of stretching exercise of posterior shoulder capsule, passive stretching exercise, will be done only 3 times with holding time 30 sec and 10 sec rest period between repetitions , strengthing exercise consists of 3 exercises all have been recommended as essential for any shoulder rehabilitation program. These exercise include shoulder flexion, scaption and horizontal extension. for each exercise, a 10-repetition maximum for 3 sets with 60 sec rest between every set + TENS and hot back.

Treatment groups

69 Participants
are divided into 3 treatment groups
Group A: High-intensity Laser TherapyExperimental treatment 2 interventions
Group B: Extracorporeal Shock WaveExperimental treatment 2 interventions
Group C: conventional therapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

supraspinatous tendon thickness

supraspinatus tendon thickness will be assess by ultrasonography.The tendon often appears swollen or thickened (frequently \> 6 to 7 mm)

Time frame
up to 6 weeks
2

supracromial space

supracromial space will be measured by ultrasonography. A normal resting subacromial space generally ranges from 9 to 11 mm. A measurement of less than 6 mm is often pathological

Time frame
up to 6 weeks
3

occupation ratio of subacromial space

The ratio comparing the thickness of the supraspinatus tendon to the overall acromiohumeral distance. An increased occupation ratio (i.e., a thickened tendon taking up too much of the space) indicates a higher risk of impingement

Time frame
up to 6 weeks

Secondary outcomes

1

pain intensity

visuala analogue scale will be used to assess pain intesity. it is a line of 100 mm.The ends are labeled with extremes, such as "No pain" at 0 mm and "Worst pain imaginable" at 100 mm.

Time frame
up to 6 weeks
2

shoulder range of motion

the range of motion will be measured by electrogoniometer

Time frame
up to six weeks
3

upper limb disability

The QuickDASH will be used to assess upper limb function.the QuickDASH is an 11-item questionnaire used to measure physical function and symptoms in people with upper limb disorders. Scores range from 0 (no disability) to 100 (most severe disability).

Time frame
up to six weeks
4

supraspinatus muscle strength

supraspinatus muscle strength will be measured by handheld dynamometer

Time frame
up to six weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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