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A Case Control Observational Study to Evaluate the Role of Excessive Fasting, Walking, Exercise, and Physical Strain in Knee Osteoarthritis among Adults Aged 40 to75 Years.

An Observational case control study on Langhan, Atyadhva, Vyayam ,Ativichestita as an Etiological factor for Janusandhigat Vata w.s.r. to E.S.R. in the age group of 40 to 75 years. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/101099
Enrollment
110
Registered
2026-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants will be selected based on the following criteria 1. Individuals aged 40 to 75 years. 2. Patients presenting with clinical features (lakshanas) of JanuSandhigata Vata, such as Vaatpurna Druti Sparsha (Sensation on palpation like a bag)filled with air. Aakunchana Prasaran Pravritti Vedana (Pain during flexion)and extension of the knee joint. Sandhi Aatopa (Crepitus in the joint). 3. Patients willing to participate in the study and provide written informed consent. 4. Patients fit for the required clinical and laboratory investigations.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they meet any of the following conditions 1. History or clinical evidence of traumatic injury to the knee joint. 2. Presence of inflammatory joint disorders such as Rheumatoid Arthritis, Gout, Septic Arthritis, or Psoriatic Arthritis. 3. Secondary osteoarthritis due to congenital, metabolic, or endocrine disorders. 4. Severe systemic illness (e.g. uncontrolled diabetes, hypertension, cardiac disease) that may interfere with study participation. 5. Patients with active infections, malignancy, or debilitating neurological disorders affecting the lower limb. 6. Pregnant or lactating women. 7. Individuals unwilling or unable to provide informed consent.

Design outcomes

Primary

MeasureTime frame
The following parameters will be recorded before and after treatment 1. Vaatpurna Druti Sparsha Shotha (Sensation of swelling on palpation, resembling a sac filled with air.) 2. Aakunchana Prasaran Pravritti Vedana (Pain experienced during flexion and extension of the knee joint.) 3. Sandhi Aatopa (Presence of crepitus in the joint.)Timepoint: At Baseline—

Secondary

MeasureTime frame
1. Erythrocyte Sedimentation Rate (ESR) Measured to evaluate inflammatory activity.. 2. Swelling Measurement Circumference of the knee joint measured with a measuring tape to detect changes in swelling. Timepoint: At Baseline—

Countries

India

Contacts

Public ContactDr Sanjay Pawade

DMM Ayurved Mahavidyalaya, Yavatmal

dr.sanjaypawade@gmail.com9822933273

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026