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A clinical study to see the effect of Ayurvedic drug in the management of Karnasrava w.s.r. to C.S.O.M.

A randomised clinical trial of Karnapichu with Gandhaka Taila, Karnadhupana and Rasnadi Guggulu in the managemaent of Karnasrava w.s.r. to chronic suppurative otitis media (C.S.O.M.)

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019914
Enrollment
30
Registered
2019-06-27
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: H661- Chronic tubotympanic suppurative otitis media

Interventions

Intervention1: Karnapichu with Gandhaka Taila along with Rasnadi Guggulu: Karnapichu (8 to 16 drops) twice a day for 30days and Rasnadi Guggulu (500 mg)twice daily for 30 days Control Intervention1: K

Sponsors

National Institute Of Ayurveda Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with signs and symptoms of karnasrava described as per Ayurvedic and modern parlance

Exclusion criteria

Exclusion criteria: 1. Age below 8 years and above 60 years. 2. Systemic diseases like uncontrolled DM, Meningitis,Tuberculosis,HTN etc 3. History of long term intake of ototoxic drugs 4. C.S.O.M. with complications like acute mastoiditis, petrositis, facial paralysis, adenoids, tonsilitis, labyrithitis etc. 5. Pregnant women.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Karnapichu with Gandhaka Taila,Karnadhupana and Rasnadi Guggulu in the management of Karnasrava(C.S.O.M.)Timepoint: 2 months

Secondary

MeasureTime frame
Any adverse event reported voluntarily, observed or enquired.Recurrence in sign and symptoms of Karnasrava(C.S.O.M.)Timepoint: 2 Months

Countries

India

Contacts

Public ContactDr Meena Nagar

National Institute Of Ayurveda

pamnani.gulab@gmail.com9461154942

Outcome results

None listed

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