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Evaluating the efficacy of electroacupuncture in comparison with physiotherapy for reducing pain and disability in soldiers diagnosed with patellar chondromalacia

Evaluating the efficacy of electroacupuncture in comparison with physiotherapy for reducing pain and disability in soldiers diagnosed with patellar chondromalacia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180416039323N4
Enrollment
40
Registered
2023-09-18
Start date
2023-08-23
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chondromalacia patellae. Chondromalacia patellae

Interventions

Intervention 1: Intervention group: In the electroacupuncture group, the patients lie on the bed and the treatment is performed at acupuncture points ST34, ST36, ST38, SP9, SP10, and GB34 with 30 x 0.

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 35 Years

Inclusion criteria

Inclusion criteria: The presence of chondromalacia patella on the basis of patient's history The course of the disease more than 2 months Failure to improve with conservative treatment for at least one month

Exclusion criteria

Exclusion criteria: History of lower limb surgery History of serious knee trauma in last 6 months or mild trauma in last 2 months The presence of any evidence of internal or external damage to the knee joint by examination or X-ray History of corticosteroid usage History of any systemic disease such as diabetes, rheumatoid arthritis Scar at the acupuncture site The presence of any deformity in the knee joint such as genovarum/genovalgum

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the intervention, 3 months after the intervention. Method of measurement: The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 (‘no pain’) and 10 (‘pain as bad as it could possibly be’).;Disability. Timepoint: Before the intervention, 3 months after the intervention. Method of measurement: The Visual Analogue Scale (VAS) measures disability intensity. The VAS consists of a 10cm line, with two end points representing 0 (‘no disability ’) and 10 (‘disability as bad as it could possibly be’).;Knee Injury and Osteoarthritis Outcome Score (KOOS) Questionnaire. Timepoint: Before the intervention, 3 months after the intervention. Method of measurement: This questionnaire is designed to measure knee pain, symptoms, motor function problems in daily activities, sports, recreation and quality of life in the knee joint. It has 42 patient-centered questions, which examines 5 concepts related to the patient. The subjects used a 5-point Likert scale. There are five options for each question, and the answers are scored from 0 to 4, and the total points obtained in each sub-group are calculated from 0 to 100 points. The number zero indicates the maximum problem and the number 100 indicates the absence of the problem.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Rezasoltani

Artesh University of Medical Sciences

z.rezasoltani@ajaums.ac.ir+98 21 4382 3476

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026