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Investigation of the synergistic effects of Multiple Drilling and Magneto-therapy on Knee Osteochondritis Dissecan.

Not Applicable
Recruiting
Conditions
Knee Osteochondritis Dissecan.
Osteochondritis dissecans
M93.2
Registration Number
IRCT20200819048462N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
36
Inclusion Criteria

Patients with grade I, II knee osteochondritis dissecan, based on Dipaola classification system
Patients with age range of 18 to 45 years

Exclusion Criteria

History of ligament or meniscus injury that has caused a major problem for the patient.
Fracture history in the last 4 weeks.
Morphine consumption for more than 3 months.
Osteoarthritis caused by inflammatory diseases including rheumatoid arthritis (RA), gout, Chondrocalcinosis and...
History of any surgery around the knee.
History of intra-articular knee injection in the last 6 months.
The patient has severe pain or dysfunction.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before any intervention (surgical or pharmaceutical), 3 and 6 months after the first evaluation. Method of measurement: Visual Analogue Scale (VAS) (0 to 10).;Functional level. Timepoint: Before any intervention (surgical or pharmaceutical), 3 and 6 months after the first evaluation. Method of measurement: According to grading the Tegner Lysholm knee scoring scale.;Knee injury and osteoarthritis outcome. Timepoint: Before any intervention (surgical or pharmaceutical), 3 and 6 months after the first evaluation. Method of measurement: Knee injury and Osteoarthritis Outcome Score (KOOS).;Quality of life. Timepoint: Before any intervention (surgical or pharmaceutical), 3 and 6 months after the first evaluation. Method of measurement: The 36-item short form health survey questionnaire (SF-36).
Secondary Outcome Measures
NameTimeMethod
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