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A Clinical Study to determine the effect of an Ayurvedic treatment module on the basis of prakriti of avascular necrosis patients.

A Single-Arm Clinical Study To Evaluate The Efficacy Of Ayurveda Treatment Module On The Basis Of Prakriti In The Management Of Asthimajjagata Vata (Avascular Necrosis of Femoral Head) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094956
Enrollment
63
Registered
2025-09-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: M870- Idiopathic aseptic necrosis of bone

Interventions

None listed

Sponsors

All India Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who are fit to undergo Panchkarma procedures as Snehpana, Virechana & Basti Karma. 2. Age between 18 to 65 years. 3. All cases of AVN of stage I to stage IV according to FICAT and ARLET classification would be considered. 4. Chronicity up to 5 yrs 5. Confirmed diagnosis of Avascular Necrosis of the femoral head with MRI Findings. 6. Both genders, male and female, will be considered for the Study

Exclusion criteria

Exclusion criteria: 1. Known cases of uncontrolled diabetes and hypertension, Tuberculosis, or severe illness 2. Pregnant or lactating mother. 3. Patients unfit for Snehpaan, Swedan, Virechana, and Basti Karma. 4. Psychiatric or cognitive impairment.

Design outcomes

Primary

MeasureTime frame
Reduction In Pain (VAS Score) Increase in Range of movement Timepoint: at baseline, after 4 week, after 8 week, after 12 week.

Secondary

MeasureTime frame
Changes in serum level of RANKL BIOMARKER & Improvement in Degenerative changes in MRI Findings. Overall improvement in quality of life. Timepoint: at baseline & after 12 weeks

Countries

India

Contacts

Public ContactDr Vikas Kumar Gothwal

All India Institute of Ayurveda

drprasanthd@gmail.com9895174060

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026