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study to find out the effectiveness of the ayurvedic drug darvyadi kashay syrup in disease tonsillitis which is called tundikeri as per ayurveda in comparision with the effect of betadine gargle in the same disease.

Randomised controlled clinical trial on efficacy of darvyadi kashay in tundikeri with special refrence to tonsillitis in children age group 6 to 12 years - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078584
Enrollment
60
Registered
2024-12-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: J039- Acute tonsillitis, unspecified

Interventions

None listed

Sponsors

Shree saptshrungi Ayurved mahavidhyalaya and hospital kamalnagar hirawadi nashik 422003
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1patients presenting with two or more symptoms like kanthshotha todavatvedana ragatva asyavairasya galoprodha as described in the context of tundikeri 2 children of age group 6 to 12 years either gender irrespective of caste and religion 3 chronic and recurrent tonsillitis

Exclusion criteria

Exclusion criteria: 1patient suffering from infectious disease 2 patient with peritonsillar abscess tonsillar cyst and tonsillolith will be excluded 3 patient with known case of HIV TB and hepatitis B will be exclude

Design outcomes

Primary

MeasureTime frame
to reduce the swelling of the tonsils, to reduce the pain while swallowing,to reduce the throat congestion, to reduce the redness and uneasiness feeling in the thorat and to reduce the recurrecy of the tonsillitis in age group 6 to 12 yearsTimepoint: as follow up are set within 7 days, we will observe the patient for the above mentioned complaints and signs

Secondary

MeasureTime frame
in secondary outcome the recurrency & the signs & symptoms like pain while swallowing should be reduced & the severeness also reduce this is secondary outcome of the trialTimepoint: 7 days

Countries

India

Contacts

Public ContactDr Yogesh Shankarrao Surse

Shree Saptshrungi ayurved mahavidhyalaya kamalnagar hirawadi panchvati nashik 422003

drsurseys@gmail.com9224297523

Outcome results

None listed

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