Health Condition 1: M171- Unilateral primary osteoarthritisof knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 male and female aged between 40 and 60 years 2 Patients with unilateral knee osteoarthritis of grade I-II on Kellgren and Lawrence (K-L) radiological ( X-Ray) classification 3 Subjects with pain 4-7 on a numerical pain rating scale will be included
Exclusion criteria
Exclusion criteria: 1 Subjects with any traumatic, metabolic, infective, or rheumatic condition affecting the knee joint. 2 Subjects with pain referred from proximal joints like the hip joint, sacroiliac joint, or lumbar spine. 3 Subjects contra-indicated for treatment with laser therapy/ iontophoresis. 4 Patients who had severe OA (grade IV according to the Kellgrenâ??Lawrence system of classification). 5 Poorly controlled diabetes mellitus with fasting blood sugar greater than 11.1 mmol/L. 6 History of anticoagulation therapy. 7 History of prior total knee replacement surgery. 8 Any dermatological problems
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| â?¢Knee ROM in flexion will be determined in prone position using a Goniometer. Pain intensity will be assessed by Visual analog scale â?¢Pain will be measured using a 10 cm VAS. â?¢The WOMAC questionnaire is used to evaluate a patientâ??s functions when diagnosed with rheumatic diseases, especially knee OA. â?¢The Medical Outcome System (MOS) sleep scale will be used to take assessment of sleep at the beginning and end of the study Timepoint: baseline immediately following intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| WOMAC QUESTIONNAIRE Medical outcome system sleep scale Timepoint: Baseline Immediately following intervention | — |
Countries
India
Contacts
Delhi Pharmaceutical Sciences and Research University