1. THE EFFICACY AND SAFETY OF CARMOLIS GEL IN THE COMBINATION THERAPY OF KNEE OSTEOARTHRITIS: RESULTS OF A MULTICENTER CLINICAL TRIAL
- Author
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I. N. Denisov, I. A. Zborovskaya, B. V. Zavodovsky, B. A. Alikhanov, I. V. Karapetyan, V. A. Shalygina, V. E. Budushkina, O. Yu. Vakulenko, A. D. Nasrullaeva, V. N. Sorotskaya, E. A. Leonova, A. I. Mironcheva, and D. V. Goryachev
- Subjects
education.field_of_study ,medicine.medical_specialty ,WOMAC ,Massage ,business.industry ,Visual analogue scale ,Immunology ,Population ,Osteoarthritis ,Diseases of the musculoskeletal system ,medicine.disease ,Rheumatology ,knee osteoarthritis ,carmolis gel ,RC925-935 ,Synovitis ,Internal medicine ,Joint pain ,Immunology and Allergy ,Medicine ,medicine.symptom ,education ,business - Abstract
Osteoarthritis (OA) is one of the most common rheumatic diseases. Knee OA is particularly frequently encountered among all forms of OA, the prevalence of knee OA being about 25% in the general population. Despite multiple guidelines for the management of knee OA, which have been prepared by the European League Against Rheumatism (EULAR), the American College of Rheumatology (ACR), and the Osteoarthritis Research Society International (OARSI), many problems of its treatment policy remain to be solved. The same holds true for not only the symptomatic and disease-modifying effects of chondroprotectors, but also topical therapy options. Objective : to evaluate the clinical efficacy and safety of Carmolis gel in patients with knee OA. Subjects and methods. The trial included 280 patients with knee OA (a study group consisted of 190 patents; a control group comprised 90 patients). The mean age was 58.3±9.3 years in the study group and 59±10.5 years in the control group. The disease duration was 10.3±5.5 and 10.1±4.1 years, respectively. Carmolis gel was applied to the region of the most painful knee joint up to 4–5 times daily, followed by massage of this skin area. The treatment cycle lasted for 2 weeks. No therapy was performed in the control patients. The clinical efficacy was determined by the changes in joint pains at rest or on movement and palpation, according to a visual analogue scale (VAS), WOMAC questionnaire, the synovitis intensity (assessed by ultrasonography), patient and physician global assessments of disease activity (Likert scale), and the possibility of reducing the daily dosage of nonsteroidal anti-inflammatory drugs (NSAIDs). The onset the therapeutic effect of the gel and the duration of its action were recorded. Results and discussion. The topical application of Carmolis gel caused a statistically significant reduction in joint pain at rest and on movement from 57.7±6.8 to 12±1.8 mm (р < 0.01) and from 52±5.3 to 17±2.7 mm, respectively (р
- Published
- 2016