A clinical trial to study the effect of trial drug panja lavana parpam(Internal),lahu vatha kesari thylam (External)on Azhal keel vayu(Osteo arthritis)

Phase 2

Recruiting

• Conditions: Pain in both knee joints swelling in kneetenderness stiffness in one are both knee jointCrepituswarmthRestricted movement of joint

• Registration Number: CTRI/2018/03/012861
• Lead Sponsor: Dr S Neelavathi

Brief Summary

Phase IIcriteria based clinical study to evaluate the clinical efficacy of siddha herbomineral formulation of Panja lavana parpam 1 Kalanju (5.1Gram) Bd with Â¼ Perungayam added toHoney (Internal) andlahuvatha kesari thylam 30 ml (External) on Azal keel vayu(Osteo arthritis)  for 48 daysin 40 patients during the trial period of 1 year 6 months that will beconducted in government siddha medical college palyamkottai tamil nadu theprimary out come is reducing the clinical symptoms and increasing the range ofmovements of trail drug Panja lavana parpam (Internal) and lahu vatha kesari thylam (external) the secondary outcome will be the Evaluation of siddha diagnosticparameters.

Detailed Description

Not available

Study Timeline

• Study Start: 2017-03-08
• Last Update Posted: 2018-03-27

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• 1.patients having symptoms of joint pain in one or both knee 2.joints,swelling,tenderness,stiffness,crepitation,restricted movements of joints.
• 3.patients who are willing to take x-ray before and after treatment.
• 4.patients who are willing to participate in this study with knowledge of potential risk.

Exclusion Criteria

1.systemic illness of the patient 2.Rhematoid arthritis 3.Use of narcotic drug 4.Pregnancy and lactation 5.History of trauma 6.Carcinoma patient Tuberculosis Immuno compromised patients Clinically significant abnormal laboratory values.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction In Severity Of Joint Pain,Stiffness,And Improvement In Physical Functioning And Quality Of Life	48 days

Secondary Outcome Measures

Name	Time	Method
Evaluation of siddha diagnostic parameters	48 days

Trial Locations

Locations (1)

Government siddha medical and hospital; 🇮🇳 Tirunelveli, TAMIL NADU, India

Government siddha medical and hospital

🇮🇳Tirunelveli, TAMIL NADU, India

Dr M Nasiyabanu

Principal investigator

9944506982

drnasiyaimthiyas@gmail.com