To develop and evaluate the efficacy of fumigation device of external auditory canal in the management of ear discharge

To develop and evaluate the efficacy of Karnadhoopan device with conventional Karnadhoopan in the management of Karnasrav with special reference to chronic suppurative otitis media a randomized controlled clinical trial

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/07/054829

Enrollment

Registered

2023-07-06

Start date

Unknown

Completion date

Unknown

Last updated

2023-07-25

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

Conditions

Health Condition 1: H660- Acute suppurative otitis media

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with features of karnasrav, safe or tubotympanic chronic suppurative otitis media without complications

Exclusion criteria

Exclusion criteria: Patients aged below 10 years and above 60 years Attic, marginal and total perforation of tympanic membrane Patients with severe conductive sensorineural and mixed deafness Patients with blood stained ear discharge Ear discharge associated with complications and other systemic disorders Advancement of disesase with pre malignant or malignant changes

Design outcomes

Primary

Measure	Time frame
Patients will have improve in ear dischargeTimepoint: first day, 15th day and 21st day	—

Secondary

Measure	Time frame
Patients will have improve in earache, itching and impaired hearingTimepoint: Day 7 Day 14 Day 21	—

Countries

India

Contacts

Public ContactDr Radhika Gandhi

Parul Institute of Ayurved ,Parul University

manjirikeskar@gmail.com9822606358

Outcome results