DEVELOPMENT AND EVALUATION OF EFFICACY OF MODIFIED SAMUDRAFENA VARTI(EAR PACKING) IN THE MANAGEMENT OF KARNASRAVA(DISCHARGE THROUGH EAR) WITH SPECIAL REFERENCE TO CHRONIC SUPPURATIVE OTITIS MEDIA

An open labelled randomized controlled clinical trial to evaluate the efficacy of modified samudrafena varti in karnasrava w.s.r to CSOM. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084944

Enrollment

Registered

2025-04-16

Start date

Unknown

Completion date

Unknown

Last updated

2025-10-13

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

Conditions

Health Condition 1: H720- Central perforation of tympanic membrane

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: AGE - Above 5 yrs 1- Patient having clinical signs and symptoms of Chronic Suppurative Otitis Media (Tubotympanic or Safe perforation).,

Exclusion criteria

Exclusion criteria: 1-Attic, marginal and total perforations of tympanic membrane 2-Patient with severe conductive, sensory-neural and mixed hearing. 3-Patient with blood-stained ear discharge. 4-Ear discharge associated with systemic disorders. Advancement of disease with pre-malignant or malignant changes

Design outcomes

Primary

Measure	Time frame
To analyse the efficacy of newly developed Modified Samudrafena Varti in management of Karnasrava with special reference to Chronic Suppurative Otitis Media as compared to conventional karnadhoopan procedureTimepoint: At baseline on 7th day and 15th day	—

Secondary

Measure	Time frame
To get relief from symptoms of karnasravaTimepoint: 14 days	—

Countries

India

Contacts

Public ContactDr Manjiri Keskar

Parul Institute Of Ayurveda

manjirikeskar@gmail.com9822606358

Outcome results