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A clinical trial to study the effect of Ayurvedic and Allopathic Treatment in the patients of Knee Osteoarthritis

Not Applicable
Conditions
Health Condition 1: M170- Bilateral primary osteoarthritis of kneeHealth Condition 2: M170- Bilateral primary osteoarthritis of knee
Registration Number
CTRI/2020/07/026737
Lead Sponsor
central council for research in ayurvedica sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients fulfilling the Revised ACR 2016 criteria of Knee OA

2.Patients presenting with classical signs & symptoms of Osteoarthritis Knee

3.Patientsâ?? age group between 50 years to 70 years irrespective of sex, religion, occupation and socioeconomic status.

4.Pain severity scale on VAS between 1 to 6 (i.e. mild to moderate)

5.Patients with BMD range of > -1.0 to -3.0

6.Patient with BMI >18.5 to <29.9

7.Patients who are willing to this trial.

Exclusion Criteria

1.Patients not fulfilling the Revised ACR 2016 criteria of Knee OA

2.Patients not fulfilling the classical sign and symptoms of OA.

3.Patientâ??s age group < 50 and > 70 years.

4.Patients with BMD range of < -3.0

5.Patient with BMI <18.5 to >29.9 (WHO)

6.Pain severity scale on VAS <1 and >6.

7.Patients having systemic disorder (Diabetic mellitus, Hypertension and other illness ) which might interfere with the treatment.

8.Patient of Autoimmune disorders, metabolic joint disorders or other than OA.

9.Patients with infective Neoplastic and traumatic condition of Knee joint.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Any change in western Ontario and McMaster University osteoarthritis (WOMAC) score from baseline to the end of 3rd, 6th and 9th weeks of follow upsTimepoint: 63days
Secondary Outcome Measures
NameTimeMethod
ï?§Assessment of changes in (clinical symptoms) subjective parameters and objective parameters from baseline to the end of 3rd, 6th and 9th weeks. <br/ ><br>ï?§Assessment of quality of life by using World Health Organization Quality of life (WHOQOL) BREF questionnaire.Timepoint: 63days
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