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Bilva taila karnapoorana with Brahmi ghrita orally in the management of tinnitus

â??A randomized open labelled controlled clinical study to evaluate the efficacy of Bilva Taila Karnapoorana with Brahmi Ghrita orally in the management of Karnanada and Karnakshweda with special reference to Tinnitus ?

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049235
Enrollment
30
Registered
2023-01-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: H931- Tinnitus

Interventions

None listed

Sponsors

Dr Mohammed Irfan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects within the age of 21 to 60 years irrespective of gender, occupation, religion, socio- economic status and duration of illness. 1. Subjects having mild to moderate hearing loss. 2. Subjects who fulfill the diagnostic Criteria. 3. Subjects willing to participate in the study with written informed consent, which is conveyed in the language which the subject can understand. 4. Subjects with tinnitus who were not undergoing treatment for tinnitus in the last six months.

Exclusion criteria

Exclusion criteria: 1. Subjects having perforated tympanic membrane. 2. Subjects having any uncontrolled systemic illness which can interfere with the course of disease and treatment. 3. Subjects having congenital deformity of ear. 4. Subjects diagnosed with other diseases like tumors of ear, Aneurysms of carotid artery, Meningitis, Meniereâ??s disease, Acute suppurative otitis media and Chronic suppurative otitis media. 5. Subjects with hearing aids, hearing asymmetry or retro cochlear pathology, metabolic or psychiatric diseases. 6. Subjectsâ?? incapable of filling/answering Tinnitus Handicap Inventory, Clinical Global Impression of Improvement (CGI-I) scale. 7. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
1. karnanada (noise in the ear) 2. karnapratinaha 3.Tinnitus handicap inventory,Tinnitus Handicap Inventory SEVERITY SCALE 4.Clinical Global Impression of Improvement (CGI-I)Timepoint: 1. 0th day â?? Pre- study Assessment 2. 7th day â?? Assessment during trail period 3. 30th day - Post study assessment 4. 45th day â?? Drug free follow-up assessment.

Secondary

MeasureTime frame
Pure tone audiometryTimepoint: Pure tone audiometry will be done on 0th day and 45th day.

Countries

India

Contacts

Public ContactDr Naveen B S

Sri Sri College of Ayurvedic Science and Research

navs009@gmail.com9844991405

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026