NCT07667998

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
69

participants targeted

Target at P50-P75 for not_applicable

Timeline
9mo left

Started Jun 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress11%
Jun 2026Apr 2027

First Submitted

Initial submission to the registry

June 19, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 25, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

June 30, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 25, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 25, 2027

Last Updated

June 25, 2026

Status Verified

June 1, 2026

Enrollment Period

10 months

First QC Date

June 19, 2026

Last Update Submit

June 19, 2026

Conditions

Keywords

High-intensity Laser TherapyExtracorporeal Shock WaveTendon ThicknessChronic Supraspinatus Tendinopathy

Outcome Measures

Primary Outcomes (3)

  • supraspinatous tendon thickness

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

    up to 6 weeks

  • 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

    up to 6 weeks

  • 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

    up to 6 weeks

Secondary Outcomes (4)

  • pain intensity

    up to 6 weeks

  • shoulder range of motion

    up to six weeks

  • upper limb disability

    up to six weeks

  • supraspinatus muscle strength

    up to six weeks

Study Arms (3)

High-intensity Laser Therapy

EXPERIMENTAL

Twenty-three patients with chronic supraspinatus tendinopathy will receive high-intensity laser and conventional physiotherapy twice a week for six weeks

Other: High-intensity Laser TherapyOther: conventional therapy

Extracorporeal Shock Wave

EXPERIMENTAL

Twenty-three patients with chronic supraspinatus tendinopathy will receive extracorporeal shock wave and conventional physiotherapy twice a week for six weeks

Other: Extracorporeal Shock WaveOther: conventional therapy

conventional therapy

ACTIVE COMPARATOR

Twenty-three patients with chronic supraspinatus tendinopathy will receive conventional physiotherapy twice a week for six weeks

Other: conventional therapy

Interventions

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

High-intensity Laser Therapy

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

Extracorporeal Shock Wave

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.

Extracorporeal Shock WaveHigh-intensity Laser Therapyconventional therapy

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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)
  • The patient will report pain with resisted isometric abduction.
  • The patient will report positive Jobe's test (empty can test)

You may not qualify if:

  • Post shoulder surgery, traumatic incidents
  • Partial tears at surgery
  • Massive retracted tears at surgery
  • Frozen shoulder Rotator cuff tear
  • Glenohumeral or acromioclavicular arthritis
  • Implanted pacemaker
  • Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Extracorporeal Shockwave Therapy

Intervention Hierarchy (Ancestors)

Ultrasonic TherapyDiathermyHyperthermia, InducedTherapeuticsPhysical Therapy ModalitiesRehabilitation

Central Study Contacts

mahmoud shaaban, phd

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
opaque sealed envelope
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: High-intensity Laser Therapy and Extracorporeal Shock Wave
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator : mahmoud mamdouh ahmed shaaban

Study Record Dates

First Submitted

June 19, 2026

First Posted

June 25, 2026

Study Start

June 30, 2026

Primary Completion (Estimated)

April 25, 2027

Study Completion (Estimated)

April 25, 2027

Last Updated

June 25, 2026

Record last verified: 2026-06