A Clinical Study Of Kansya Shalaka Agnikarma In Vatakantaka.

A Randomized Controlled Clinical Trial To Study The Effect Of Kansya Shalaka Agnikarma In Pain Management Of Vatakantaka With Special Reference To Plantar Fasciitis - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/100523

Enrollment

Registered

2026-01-08

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: M708- Other soft tissue disorders related to use, overuse and pressure

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1) Diagnose patients exhibiting signs and symptoms of Vatakantaka, such as ruk (stiffness) and vedana (pain). 2) Target patients aged 40 60 years, regardless of religion or caste.

Exclusion criteria

Exclusion criteria: 1) Uncontrolled diabetes, hypertension, HIV, cardiac disease, cancer, or TB. 2) Local skin infection at the Agnikarma site. 3) Calcaneal stress fracture. 4) Anarha (unsuitable candidates) of Agnikarma.

Design outcomes

Primary

Measure	Time frame
Reduction in heel pain intensity in patients of Vatakantaka after Kansya Shalaka AgnikarmaTimepoint: 7 days	—

Secondary

Measure	Time frame
Where the trial group stands in comparison with control groupTimepoint: 18 months	—

Countries

India

Contacts

Public ContactDr Nikita Lalasaheb Elajale

SMBT Ayurved College And Hospital

drsmitaaher52@gmail.com9764700610

Outcome results