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Effect of Vidangadi Dhoompana with Shadbindu taila Nasya and Elakanadi kwatha in the management of Chronic rhinosinusitis

Add on effect of Vidangadi Dhoompana with Shadbindu taila Nasya and Elakanadi kwatha in the management of Dushta Pratishyaya Chronic rhinosinusitis an open label double arm randomized control clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088768
Enrollment
46
Registered
2025-06-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

None listed

Sponsors

All India Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients presenting with clinical features of Dustha Pratishyaya as per classic irrespective of sex caste or religion 2 Patients with signs and symptoms of Chronic Rhinosinusitis 3 Patients in the age group of 21 to 60 years with history of sinusitis of more than 12 weeks

Exclusion criteria

Exclusion criteria: 1 Patients not willing to participate in clinical trial 2 Chronic debilitating infectious diseases 3 Cases with nasal polyp requiring surgical treatment 4 Patients associated with nasal and PNS carcinoma

Design outcomes

Primary

MeasureTime frame
Changes in Shirashoola Nasavrodha Shirogaurava Nasasrava Gandhat na veti etcTimepoint: After completion of 4 weeks of intervention patient will be followed for 4weeks once in two weeks Follow up of the patients will be ensured by telephonic communication or by creating a WhatsApp group The compliance of the patient will be noted in a separate sheet provided to them

Secondary

MeasureTime frame
1 Changes in the haematological findings ie TLC DLC ESR and Hb Absolute Eosinophil count 2 Changes in investigations X RAY of (PNS) Timepoint: After completion of 4 weeks of intervention patient will be followed for 4weeks once in two weeks

Countries

India

Contacts

Public ContactDr Ashish Kumar Verma

All India Institute of Ayurveda New Delhi

drpankajkundal@yahoo.com7291887810

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026