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Use of ayurvedic formulation in otomycosis

Randomized controlled clinical trail to evaluate the efficacy of karnamayaghna taila karnapooran in karnakandu with special reference to otomycosis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070883
Enrollment
70
Registered
2024-07-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: H618- Other specified disorders of external ear

Interventions

None listed

Sponsors

Dr Sneha Prakash Patil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients having signs and symptoms of Karnakandu with special reference to otomycosis.2)Patients between 18-50 years of age group, irrespective of gender,caste, religion, economical class,race.3)Intact tympanic membrane after aural cleaning.

Exclusion criteria

Exclusion criteria: 1)Patients having Karnakandu with other than ear pathology as ASOM,CSOM, perforation of tympanic membrane and patients other than Karnakandu will be excluded.2)Patients below 18 and above 50 years of age group.3)Patients having systemic disease with complications which can lead to interference twith the study.4)Mentally retarded patients.5)Congenital anomalies of the ear.

Design outcomes

Primary

MeasureTime frame
To decrease the sign and symptoms of otomycosis Timepoint: 15 days study with follow up on 5th,10th, 15th,30th day (0,5,10,15,30 days)

Secondary

MeasureTime frame
To study the adverse effect of ayurvedic formulation,if anyTimepoint: 15 days study with follow up on 5th, 10th, 15th, 30th day (0,5,10,15,30 days)

Countries

India

Contacts

Public ContactDr Sneha Patil

LRP ayurvedic medical college and hospital and PGT and RC Islampur

drneetapatil@rediffmail.com9527525654

Outcome results

None listed

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