Not Yet RecruitingNot Applicable

Effect of Pulsed Electromagnetic Field on Pruritus in Burn Scars

40 participantsStarted 2026-03-01

Plain-language summary

This study will be conducted to evaluate the effectiveness of pulsed electromagnetic field therapy in pruritus in patients with burn scars.

Who can participate

Age range

25 Years – 40 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 aged 25-40 years. * Patients with second and third-degree burn scars sustained at least 3 months prior to enrollment. * Patients experiencing a pruritus score ≥ 5 on the Visual Analog Scale (VAS). * Patients who have not undergone prior PEMF therapy or other physical therapy interventions for pruritus in the past 3 months. Exclusion Criteria: * Patients with cardiac pacemakers, implanted defibrillators, or other electronic medical devices. * Pregnant or lactating women. * Patients with uncontrolled systemic diseases (e.g., diabetes, hypertension) or active skin infections. * Patients with psychological disorders that would interfere with their ability to adhere to the treatment protocol. * Patients with allergic reaction to food or drugs

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.

What they're measuring

pain intensity

Timeframe: up to 6 weeks

life disability

Timeframe: up to 6 weeks

Trial details

NCT IDNCT07443358

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-06-01

Contact for this trial

Asmaa Eliwa, master

01150761961 dr.asmaa1812@gmail.com

View on ClinicalTrials.gov More Burn Scar trials

Who can participate

Age range

25 Years – 40 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.