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A Study to know the effect of Siddha medicine BavanaKadukkai (internal) and Sirasunoi peenisamsirasoolaiku thailam(mudithailam) in the treatment of peenisam (sinusitis)

An Open Clinical Trial to evaluate the effectiveness of Siddha formulations Bavanakadukkai (Internal) and Sirasunoi peenisamsirasoolaiku thailam (mudithailam) in the management of peenisam (sinusitis) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072776
Enrollment
30
Registered
2024-08-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: J329- Chronic sinusitis, unspecified

Interventions

Intervention1: Bavanakadukkai(Internal) Sirasunoi peenisamsirasoolaiku thailam(mudithailam): A Compound herbal drug tablet indicated to treat sinusitis advised to intake one tablet chewable before an

Sponsors

National Institute Of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults who are already diagnosed with sinusitis are included Patient who has SNOT-22 Score above20 Patient who has radiological evidence of sinusitis

Exclusion criteria

Exclusion criteria: Migraine Patients who have tumours in PNS X-ray Pregnancy and lactating mother Patient with uncontrolled diabetes mellitus HBA1C 8.2 and hypertension systolic bp more than 180 and diastolic more than 110mmHg Patient who are not willing to participate in the study will be excluded in this study

Design outcomes

Primary

MeasureTime frame
The outcome will be mainly assessed by reduction in clinical symptoms after the treatment by using sino- nasal outcome test-22Timepoint: 48 days

Secondary

MeasureTime frame
Observe changes in clinical lab parameters ESR IgE AEC Pre and Post treatmentTimepoint: 48 days

Countries

India

Contacts

Public ContactDr H Nalini Sofia

National Institute of Siddha

drhnalinisofia@gmail.com8939899363

Outcome results

None listed

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