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Effect of Pathadi Taila Nasya and Vyaghri Haritaki Avaleha in Paranasal Sinusitis.

Evaluation of Comparative Efficacy of Pathadi Taila Nasya along with Vyaghri Haritaki Avaleha versus Anu Taila Nasya and Vyaghri Haritaki Avaleha in the management of Nasavivar Shotha (Paranasal Sinusitis): A Randomized Control Trial. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079308
Enrollment
74
Registered
2025-01-23
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: 3- Administration

Interventions

None listed

Sponsors

Dr Suraj Sadashiv Patlekar
Lead Sponsor
Dr Suraj Sadashiv Patlekar
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with signs & symptoms of Nasavivar Shotha (Paranasal Sinusitis) & fulfilling the criteria for Sinusitis set by the American Academy of Otolaryngology, Head & Neck Surgery (AAO-HNS). Patients whose medical history along with physical examination, radiographic findings (Opacification/haziness of Sinus with Mucosal Thickenings; Air Fluid Level) suggested paranasal sinusitis i.e Caldwell/Waters View.

Exclusion criteria

Exclusion criteria: - Unwilling patients for trial/giving written consent. - Patient requiring Surgical/ other Interventions. - Pregnant ladies/ Lactating mothers. - Patients having/diagnosed cases of Diabetes, Hypertension, Hepatic Disease, Renal Disorders, Metabolic & GIT disorders, Poor Health Status, Malignancy, Tuberculosis, AIDS or other major Systemic Disorders. - Hypersensitivity to any of the trial medicines.

Design outcomes

Primary

MeasureTime frame
To study the comparative efficacy of Pathadi Taila Nasya alongwith Vyaghri Haritaki and Anu Taila Nasya along with Vyaghri Haritaki Avaleha in the management of Nasavivar Shotha (Paranasal Sinusitis). Timepoint: 60 Days

Secondary

MeasureTime frame
1) Improvement in the clinical features of Nasavivar Shotha in Grading/Scoring.All subjective criteria will be recorded for score in each & every patient before & after treatment. 2) Improvement in the objective parameters with the help of CT SCAN PNSTimepoint: 60 days

Countries

India

Contacts

Public ContactDr Suraj Sadashiv Patlekar

Datta Meghe Institute of Higher Education and Research (Deemed to be University)

sjain_med@yahoo.co.in9881836366

Outcome results

None listed

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