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An interventional study comparing shirobasti and Shiroabhyanga with ksheerabala taila in 40 patients with facial paralysis(ardita)

A Randomised Comparative clinical study to Evaluate the effect of Shirobasti and Shiroabhyanga with Ksheerabala taila in ardita - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102072
Enrollment
40
Registered
2026-01-27
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: G51- Facial nerve disorders

Interventions

None listed

Sponsors

Dr Shurekha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient having classical signs & symptoms of Ardita 1.Mukha Vakrata 2.Vak Sangh 3.Nethra Stabdhata 4.Lala Srava 5.Karna Shoola 6.House Brackmann Scale

Exclusion criteria

Exclusion criteria: 1.Pregnant women and lactating mother 2.Patients with any other systemic disorder that interfere with the course of treatment 3.Patients who are contraindicated for Murdhini Taila.

Design outcomes

Primary

MeasureTime frame
Symptoms ReducedTimepoint: 2 weeks

Secondary

MeasureTime frame
Overall improvement of sleep and general heathTimepoint: 2 weeks

Countries

India

Contacts

Public ContactDr Ashwini a sangoli

Shree shivayogeshwara rural ayurvedic medical College and hospital Inchal

aksshetty402@gmail.com8892209106

Outcome results

None listed

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