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DEVELOPMENT OF A CLINICAL PREDICTION RULES TO IDENTIFY EFFICACY OF PULSED ELECTROMAGNETIC THERAPY ON BURN WOUND HEALING

Cairo University (CU) logo

Cairo University (CU)

Status

Active, not recruiting

Conditions

Burn Wound

Treatments

Device: electromagnetic device

Study type

Interventional

Funder types

Other

Identifiers

NCT05341427
P.T.REC/012/003534

Details and patient eligibility

About

The purpose of this study is to investigate whether patients' age, total burned surface area, wound stage and wound depth determine wound healing response to pulsed electromagnetic therapy in burn patients

Full description

It will be hypothesized that

  1. Age may significantly affect burn wound healing's response to pulsed electromagnetic waves.
  2. TBSA may significantly affect burn wound healing's response to pulsed electromagnetic waves
  3. Depth of wound may significantly affect burn wound healing's response to pulsed electromagnetic waves
  4. Wound healing stage may significantly affect burn wound healing's response to pulsed electromagnetic waves This study will be conducted at the in-patient burn units. There will be only one intervention group. The duration of the study will be 6 weeks divided to 18 sessions (three sessions per week). Sixty patients (male and female) will be recruited from the burn units.

Pulsed electromagnetic waves will be performed for 60 min 3 times per week till healing (maximum 8 weeks) on the wound area.

PEMF therapy will be as (duration: 60 minutes; frequency: 12 Hz; intensity: 12 Gauss)

Enrollment

60 estimated patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria Partial thickness Burn wound depth. Age ranges from 20-50 years. TBSA more than 15% Sufficient understanding to perform the tests. Exclusion Criteria Diabetic patients. Patients receiving immunosuppressive drugs. Associated co-morbidities, such as neurological diseases, malnutrition, and other inflammatory and/or infectious diseases.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

burn wound receiving electromagnetic therapy
Experimental group
Description:
There will be only one intervention group. The duration of the study will be 6 weeks divided to 18 sessions (three sessions per week). Sixty patients (male and female) will be recruited from the burn units of Cairo university hospitals
Treatment:
Device: electromagnetic device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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