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Ayurvedic nasal treatments using herbal paste, medicated oil drops, and oral tablets to relieve nasal blockage, loss of smell, sneezing, and runny nose in patients with nasal mass.

A CLINICAL STUDY ON THE EFFICACY OF CHITRAKA KSHARA PRATISARANA KARAVIRADHYA MARSHA NASYA AND KSHARA GUTIKA IN NASA ARSHA WITH SPECIAL REFERENCE TO NASAL POLYPOSIS A SINGLE ARM STUDY - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099472
Enrollment
35
Registered
2025-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: J330- Polyp of nasal cavity

Interventions

None listed

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All diagnosed patients of Nasal Polyps having sign and symptoms of Nasa Arsha like Atyadhik pratishyaya, Kshyavahu, Krichho swasa-uchwasa, Putinasya, Anunasika, etc. 2. Patients aged between 16-60 years. 3. Patients with associated conditions, such as Chronic rhinosinusitis with Nasal Polyposis (CRSwNP). 4. Patients not currently on systemic corticosteroids or immunotherapy in the last 4 weeks. 5. Patients who provide informed consent for the study. 6. Able to comply with follow-ups and study protocols.

Exclusion criteria

Exclusion criteria: 1. Patient having Sinonasal malignancies (e.g., squamous cell carcinoma, adenocarcinoma), Olfactory neuroblastoma. 2. Patients who have undergone recent nasal surgery within a span of one month. 3. Patient using systemic corticosteroids. 4. Patients with uncontrolled comorbidities like Hypertension , Diabetes, Bronchial Asthma etc. 5. Patient unfit for Nasya and Kshara Pratisarana. 6. Patient who has been already in any kind of experimental drug study. 7. Patients with cognitive impairment, non-compliance, or inability to provide informed consent. 8. Systemic illness, acute URTI, fungal rhinosinusitis etc.

Design outcomes

Secondary

MeasureTime frame
Reduction in polyp size, assessed through the Endoscopic Nasal Polyp Score (NPS)Timepoint: 21 Days

Primary

MeasureTime frame
Improvement in symptoms as measured by the Sino-Nasal Outcome Test (SNOT-22) score.Timepoint: 21 Days

Countries

India

Contacts

Public ContactProf Dr Shamsa Fiaz

National Institute of Ayurveda, Jaipur, Rajasthan

shamsa_fiaz@yahoo.com8764009846

Outcome results

None listed

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