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The study to know the effect of Aragbadhadi kwatha ear cleasing along with Shaiwaladi taila soaked cotton application in patients with CSOM.

A clinical study to evaluate the efficacy of Aragbadhadi kwatha karna prakshalana with Shaiwaladi taila karna pichu in the management of karnasrava With special reference to tubotympanic Chronic Suppurative Otitis Media - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106239
Enrollment
80
Registered
2026-03-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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: Patients will be treated with Karna prakshalana using Aragbadhadi gana kwatha alongwith Shaiwaladi taila karna pichu: Patients will be treated with Karna prakshalana using Aragbadhadi

Sponsors

Government ayurvedic college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 05 to 30 years Patients having ear discharge, perforated TM impaired hearing etc symptoms at least in one ear Patients willing to give written consent Patients culture and senstivity test shows flora sensitive to ofloxacin for control group If patient having discharge in both ear I will take the one ear having moderate discharge for the study

Exclusion criteria

Exclusion criteria: Patients below the age of 5 years and above 30 yrs Patients having allergy to any of the trial or control drugs other systemic disease like TB DM HTN fungal and viral disease as well as car surgery Patients having flora resistant to ofloxacin in Culture and senstivity test for control group Patients unable to continue for duration of treatment Pregnant and lactating mother Patients suffering from atticoantral type of chronic suppurative otitis media cholesteatoma discharge due to injury and any serious complications

Design outcomes

Primary

MeasureTime frame
Observation of the result for effect of my trial at the end of trialTimepoint: 8 weeks

Secondary

MeasureTime frame
Detremination of effect of the interventon with respect to other in generalTimepoint: 6 months

Countries

India

Contacts

Public ContactArjun kumar singh

Govt ayurvedic college kadamkuan patna 3

dr.aksingh969@gmail.com9576952168

Outcome results

None listed

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