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Investigating the effect of electromagnetism in reducing knee osteoarthritis symptoms

Not Applicable
Recruiting
Conditions
Knee osteoarthritis.
Osteoarthritis of knee
Registration Number
IRCT20231007059642N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Primary diagnosis of grade 2 and 3 OA based on ACR criteria, including radiological evidence, clinical examination and history
Age =40 years
The presence of dry knee symptoms and frequent daily pain since 6 months ago
Symptomatic illness from at least 6 months ago
Presence of pain with VAS =3 criteria

Exclusion Criteria

Intra-articular drug administration in the last 6 months
Systemic treatment with corticosteroids or physical therapy in the last 6 weeks
Cartilaginous consumption in the last 6 weeks
Back radicular pains
Knee pain caused by malignant, autoimmune and inflammatory pathology or caused by knee deformities such as genovarus and genovalgus etc.
Patients who have a history of knee surgery
Lack of cooperation and difficulty in referring and following the intervention process
pregnancy
Metal implant like heart pacemaker

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Symptoms of knee osteoarthritis. Timepoint: before, immediately and 6 weeks and 3 months after the end of the treatment. Method of measurement: Visual Analogue Scale and Western Ontario and McMaster Universities Osteoarthritis Index scale.
Secondary Outcome Measures
NameTimeMethod
Average pain intensity. Timepoint: Before, immediately and 6 weeks and 3 months after the end of the treatment. Method of measurement: Visual Analogue Scale.;Physical performance. Timepoint: Before, immediately and 6 weeks and 3 months after the end of the treatment. Method of measurement: Western Ontario and McMaster Universities Osteoarthritis Index.;Joint dryness. Timepoint: Before, immediately and 6 weeks and 3 months after the end of the treatment. Method of measurement: Western Ontario and McMaster Universities Osteoarthritis Index.;Range of motion. Timepoint: Before, immediately and 6 weeks and 3 months after the end of the treatment. Method of measurement: Western Ontario and McMaster Universities Osteoarthritis Index.
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