Effect of Ozonated Gel Phonophoresis on Pain and Functional Disability in Patients With Chronic S… (NCT07316738) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Ozonated Gel Phonophoresis on Pain and Functional Disability in Patients With Chronic Supraspinatus Tendinitis
Egypt40 participantsStarted 2025-12-25
Plain-language summary
This study will be conducted to investigate the effect of ozonated gel phonophoresis on pain intensity, shoulder joint range of motion, and functional disability in patients with chronic supraspinatus tendinitis grades I and II.
Who can participate
Age range
30 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients from 30-60 years old from both genders.
* The patients will be assigned to the study will be diagnosed with grade I or II supraspinatus tendinitis based on Neer's classification.
* The patients suffered from supraspinatus tendinitis for more than 3 months and taking non-steroidal anti-inflammatory drugs suggested by orthopedist.
* All patients have body mass index between 18.5 and 29.9 kg/m2.
Exclusion Criteria:
* Grades III of supraspinatus tendinitis. (Bone spurs and tendon rapture)
* Any past shoulder surgical interventions. (Rotator cuff repair, labrum tear and open reduction internal fixation)
* Shoulder joint instability
* Shoulder fracture.
* Non-cooperative subjects.
* Neuromuscular diseases (spinal muscular atrophy, whiplash injury)
* Cardiovascular disease.
* History of cancer.
* Systemic diseases such as rheumatoid arthritis, Reiter's syndrome, or diabetes.
* Severe medical and neurological or psychiatric disorders.
* Pregnant and lactating women.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.