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To study the efficacy Of Agnikarma With Raupya Shalaka in Vatakantak with special reference to Calcaneal spur.

Randomized Controlled Clinical Trial To Evaluate The Efficacy Of Agnikarma With Raupya Shalaka in Management Of Vatakantak With Special Reference To Calcaneal Spur - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076444
Enrollment
90
Registered
2024-11-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: M773- Calcaneal spur

Interventions

None listed

Sponsors

Dr Sonali Sambhaji Katekar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient having age between 25 to 60 years. 2.Patients irrespective of gender, economic class, religion and occupation 3.Patient having sign and symptoms of padadari will be randomly selected.

Exclusion criteria

Exclusion criteria: 1.Any fracture of foot (like calcaneal fracture) 2.Patient suffering from systemic disorder like diabetes mellitus,HTN,Haemophilia etc 3.Patients suffering from infectious disease like HIV,TB etc.

Design outcomes

Primary

MeasureTime frame
Study to assess the efficacy of Agnikarma with Raupya Shalaka in management of Vatakantak with special reference to Calcaneal Spur in age group of 20 to 70 years for 21 daysTimepoint: 21 days study includes follow up on 0th,7th,14th and 21th day

Secondary

MeasureTime frame
To assess the efficacy of Agnikarma with Raupya Shalaka in the management of Vatakantak with special reference to Calcaneal spur To reduce the symptoms of VatakantakTimepoint: 21 days with f/u 7th,14th & 21st day

Countries

India

Contacts

Public ContactDr Shubhangini Suresh Nagaralmath

LRP Ayurvedic Medical College And Hospital PG Institute and Research Center urun islampur

shubhasn@gmail.com7709677061

Outcome results

None listed

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