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Effect of Electromagnetic Therapy on Patients With Chronic Rhinosinusitis.

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Rhinosinusitis
Fatigue
Magnetic Therapy
Headache

Treatments

Device: Pulsed electromagnetic field

Study type

Interventional

Funder types

Other

Identifiers

NCT05865613
magnetic and rhinosinusitis

Details and patient eligibility

About

This study aimed to evaluate the efficacy of Pulsed electromagnetic field (PEMF) for Chronic sinusitis in a randomized, double-blind, placebo-controlled trial.

Full description

Chronic sinusitis, or chronic rhinosinusitis, is an inflammatory condition defined by symptomatic inflammation of the paranasal sinuses lasting longer than 3 months. Common presenting symptoms include nasal obstruction, facial pressure or fullness, nasal discharge (anterior or posterior), and olfactory loss. Furthermore, chronic sinusitis is associated with reductions in patient quality of life, sleep quality, and daily productivity.

A pulsed electromagnetic field (PEMF) has an anti-inflammatory, antimicrobial, and improves the microcirculation of the mucosal membrane of the nasal cavity. It has been suggested that magnetic therapy can be used in treating chronic sinusitis but there is a scarce of studies about its usage.

Enrollment

37 patients

Sex

All

Ages

20 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients suffering from mild to moderate symptoms of rhinosinusitis.

Exclusion criteria

  • pregnant or breastfeeding women.
  • patients with definite deviated nasal septum, sinusitis, or history of operation within the last 6 months.
  • patients with hypertension, diabetes mellitus, malignancy, active pulmonary tuberculosis, infection, active respiratory disease like asthma, or other systemic diseases.
  • patients with long-term use of corticosteroids or immunosuppressive agents.
  • patients who were involved in another clinical study within 30 days.
  • patients who were unable to comply with the follow-up schedules.
  • patients who had used antihistamines within 1 week, topical corticosteroids within 2 weeks, systemic corticosteroids within 4 weeks, anti-cholinergic drugs within 3 days, antileukotriene drugs within 1 week, decongestants within 3 days, tricyclic antidepressants or phenothiazines within 2 weeks, non-steroidal analgesics within 2 weeks, and other drugs which the researchers believed were inappropriate.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

37 participants in 2 patient groups

Magnetic group
Experimental group
Description:
Participants were randomized into either the PEMF group or sham treatment group by a computer-generated random number. The participants were treated using PEMF (20 G,7H for 10min). treatment was delivered for one month.
Treatment:
Device: Pulsed electromagnetic field
Sham magnetic group
Sham Comparator group
Description:
Participants were randomized into either the PEMF group or sham treatment group by a computer-generated random number. The participants were treated using PEMF without adjusting the output. treatment was delivered for one month.
Treatment:
Device: Pulsed electromagnetic field

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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