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Effect of ayurvedic medicine in hearing loss

Evaluation of the effect of Lashunadi taila karnpooran and sarivaadi vati with and without Ashwagandhadhya ghrita in badhirya

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/07/015077
Enrollment
60
Registered
2018-07-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients of Badhirya

Interventions

Intervention1: use of Lashunadi taila for karnpooran and sarivaadi vati orally: patients will be given 1. Lashunadi taila karnpooran-5 ml in each ear for 10 days 2. sarivaadi vati 2 tab. BD for 2 mont

Sponsors

Patanjali Ayurvedic College
Lead Sponsor
Dr Sheweta Kotwal
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with hearing loss irrespective of gender, caste, religion and economic status. 2.Patients with the age group of 16-65 years. 3.Patients with mild to severe degree of Hearing impairment i.e. 26 dB to 91 dB (according to WHO 1980 guidelines).

Exclusion criteria

Exclusion criteria: 1.Patients with age 65 years. 2.Patients with profound degree of Hearing impairment i.e. > 91 dB (according to WHO 1980 guidelines) 3.Patients with perforated tympanic membrane. 4.Patients with otorrhoea. Patients with congenital hearing loss.

Design outcomes

Primary

MeasureTime frame
Subjective Parameters: 1.Tinnitus. 2.Giddiness. Objective Parameters: 1.Pure tone audiometry. Timepoint: Assessment to be done prior to the start of the treatment

Secondary

MeasureTime frame
Subjective Parameters: 1.Tinnitus. 2.Giddiness. Objective Parameters: 1.Pure tone audiometry. Timepoint: Assessment to be done after the completion of treatment

Countries

India

Contacts

Public ContactDr Vandana Vidyarthi

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan

vandanavidyarthi27@gmail.com7376006555

Outcome results

None listed

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