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Role OF LAGHU VISHAGARBHA TAILA AND MARMA THERAPY IN THE MANAGEMENT OF SANDHIGATA VATA w.s.r. TO OSTEOARTHRITIS

Not yet recruiting
Conditions
Osteoarthritis, unspecified site,
Registration Number
CTRI/2019/05/019131
Lead Sponsor
Uttrakhand Ayurved University
Brief Summary

Sandigata Vatais a common condition which can be correlated with osteoarthritis. Sandhigatavata  is a common type of Vatic disorderafflicting the society. Owning to distracting nature and difficult anagement atavyadhi has been included in Asht mahagad. Osteoarthritis is a joint failure, adisease in which all structures of the joint have under gone pathology change.This is accompanied by increasing thickness and sclerosis of the subchondralbony plate, by outgrowth of osteophytes at the joint margin, by stretching ofthe articular capsule, by mild synovitis in many affected joints, and by theweakness of muscles bridging the joint. OA is a long term chronic diseasecharacterized by the deterioration of cartilage in joints which result in bonesrubbing together and creating stiffness, pain and impaired movement. Thedisease most commonly affects the joints in the knees, hands, feet, and spineand is related to ageing. It is also associated with a variety of both modifiableand non-modifiable risk factors, including obesity lack of exercise, geneticpredisposition, bone density, occupational injury, trauma and gender.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

INCLUSION CRITERIA- 1.Patients fulfilling the diagnostic criteria of Sandhigata Vata (OA) 2.Patients aged between 30 -70 years will be included of either sex.

Exclusion Criteria
  • EXCLUSION CRITERIA- 1.Patients having history of joint trauma, secondary and other systemic illness.
  • 2.Patients suffering from any systemic diseases like tuberculosis, rheumatoid arthritis, gouty arthritis, psoriatic arthritis .
  • 3.Patient suffering from infectious osteoarthritis.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete remission:100% reliefComplete remission:100% relief | Markedly improved:76-99% relief | Moderately improved:51%-75% relief | Improved:26%-50% relief | Unchanged:0% – 25% relief
Markedly improved:76-99% reliefComplete remission:100% relief | Markedly improved:76-99% relief | Moderately improved:51%-75% relief | Improved:26%-50% relief | Unchanged:0% – 25% relief
Moderately improved:51%-75% reliefComplete remission:100% relief | Markedly improved:76-99% relief | Moderately improved:51%-75% relief | Improved:26%-50% relief | Unchanged:0% – 25% relief
Improved:26%-50% reliefComplete remission:100% relief | Markedly improved:76-99% relief | Moderately improved:51%-75% relief | Improved:26%-50% relief | Unchanged:0% – 25% relief
Unchanged:0% – 25% reliefComplete remission:100% relief | Markedly improved:76-99% relief | Moderately improved:51%-75% relief | Improved:26%-50% relief | Unchanged:0% – 25% relief
Secondary Outcome Measures
NameTimeMethod
Exacerbation in sign and symptom90 days

Trial Locations

Locations (1)

Rishikul Ayurvedic Hospital

🇮🇳

Hardwar, UTTARANCHAL, India

Rishikul Ayurvedic Hospital
🇮🇳Hardwar, UTTARANCHAL, India
Urvashi
Principal investigator
9761055936
urvashipanwar2009@gmail.com

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