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Pulsed Electromagnetic Field Stimulation and Charcot Foot Ulcer

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Charcot Foot Ulcer

Treatments

Device: Transcutanous electrical nerve stimulation
Device: pulsed electromagnetic field therapy
Drug: Vancomycin

Study type

Interventional

Funder types

Other

Identifiers

NCT06527131
P.T.REC/012/005154

Details and patient eligibility

About

thirty-four patients with charcot foot ulcer will be included, their ages will be ranged from 50 to 70 years old and randomly distributed into two equal groups : study group includes 17 patients who will recieve pulsed electromagnetic field and electrical stimulation three days per week for three months .

control group includes 17 patients who will recieve electrical stimulation , standard wound care and medical treatment

Enrollment

34 estimated patients

Sex

All

Ages

50 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age ranges between 50 and 70 years old male and female patients all patients with charcot foot ulcer

Exclusion criteria

  • presence of malignancy hypotensive patients pregnancy immunological and rheumatological disorders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

Group A (Study group)
Experimental group
Description:
PEMF group who recieves pulsed electromagnetic field therapy and electrical stimulation
Treatment:
Device: pulsed electromagnetic field therapy
Device: Transcutanous electrical nerve stimulation
Group B(control group)
Active Comparator group
Description:
who recieves standard wound care , electrical stimulation and medical treatment
Treatment:
Drug: Vancomycin
Device: Transcutanous electrical nerve stimulation

Trial contacts and locations

1

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Central trial contact

Nessrien AbdelRashid, assistant professor; Norhan Eltayeb, MSc candidate

Data sourced from clinicaltrials.gov

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