Clinical trial Recruiting at 1 site Interventional Ages 40 to 60

Shoulder Tendinitis: Ultrasound and Biomechanical Effects of BFRT and Eccentric Exercise

Official title: Anatomical Evaluation of Supraspinatus Through Ultrasonography and Biomechanical Measurements Following Different Combinations of Physical Therapies in Patients of Supraspinatus Tendinitis.

Run by Sehat Medical Complex · NCT07873528 · Data updated 2026-11-12

This study tests whether combining blood flow restriction therapy with eccentric exercise helps people with supraspinatus tendinitis, compared to BFRT alone, eccentric training alone, or routine physical therapy.

More Supraspinatus Tendinitis trials

Quick facts

Study typeInterventional
Ages40 Years to 60 Years
SexAll
Enrollment60 (estimated)
SponsorSehat Medical Complex
Academic / other
Locations1 site (Lahore, Punjab Province)
StatusRecruiting
StartedDecember 23, 2026
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedOctober 14, 2026
Trial IDNCT07873528 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Men and women aged 40–60 with unilateral shoulder pain and at least two positive impingement tests, a pain score of 5 or higher, and no recent physical therapy for the condition.

Probably not a fit

Individuals with full-thickness rotator cuff tears, frozen shoulder, recent shoulder surgery, or ongoing systemic or neurogenic shoulder pathology may not benefit and are excluded.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults aged 40–60 with unilateral supraspinatus tendinitis will be randomized into four groups to receive different interventions over a treatment period. Outcomes will include musculoskeletal ultrasound measures, range of motion, pain thresholds, muscle strength, and function to assess changes in tendon thickness and performance. The study uses BFRT, eccentric training, their combination, and standard physical therapy, with evaluations before and after the intervention. Safety and feasibility will be monitored, and participants will be recruited from Sehat Medical Complex in Lahore, Pakistan. Sample size is 60 participants across all groups.

Why it matters

Potential benefit: If successful, participants may experience reduced pain, improved shoulder function, and better tendon health related to supraspinatus tendinopathy.

How similar studies have gone: Past research has shown benefits from BFRT and eccentric training in shoulder conditions, but the specific combination with imaging and biomechanical endpoints in supraspinatus tendinitis is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient age 40-60 years with unilateral shoulder.
* Patient with at least two positive test (Empty Can, Hawkins-Kendy and Neer impingement test) in sitting and standing position will be enrolled.
* Patient with shoulder pain history up to three months.
* The shoulder pain on NPRS will be above or equal to 5 for the recruitment.
* Both male and female population.
* People who have not received any physical therapy treatment or exercise regimen for the past 3 months for upper limb injury or disease.

Exclusion Criteria:

* Patients with referred shoulder pain, systemic musculoskeletal pathology e.g., neurogenic, visceral referred pain.
* Full thickness tear of rotator cuff muscle or tendons.
* Patients with frozen shoulder pain or limited range of motion \< 90degree shoulder abduction.
* Patients with previous shoulder surgery, intra articular injection, nerve block to shoulder last 6 month.
* Pregnant woman or 6-month recent history of pregnancy.
* Patient with history of blood pressure \>180mmHg systolic.
* Patients with recent history of upper limb fracture, open wound, history of vascular surgery, uncontrolled diabetes and fistula in upper limb.

Where it's running

  • Sehat Medical Complex/UOL/UVAS
    Lahore, Punjab Province, Pakistan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.