Comparison between effect of bala tail and tila tail nasya,pichu,pana in nasal obstruction(nasanaha)

Phase 1/2

Not yet recruiting

• Conditions: Acute upper respiratory infection,unspecified. Ayurveda Condition: NASAROGAH,

• Registration Number: CTRI/2022/06/042996
• Lead Sponsor: Patanjali ayurvedic hospital

Brief Summary

This study is a randomized, open-labeled, parallel-group, clinical trial, to compare and evaluate effect of bala tail and tila tail nasya pichu and pana in nasanaha..

Patients suffering with symptoms of nasanaha attending the OPD/IPD of SHALAKYA TANTRA department of Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar will be selected randomly for this clinical study irrespective of sex, religion, occupation etc. A detailed Performa will be prepared on basis of Ayurvedic text and allied sciences. The patient fulfilling the inclusion and exclusion criteria will be registered on this Performa and scoring of different clinical features will be done on the assessment criteria.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-06-13
• Last Update Posted: 2022-08-31

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• 1.Patients suffering with clinical features of nasanaha (nasal obstruction) 2.
• Age group between 15 to 60 years 3.Patient having atleast 1-2 associated complaints e.g- headache, nasal discharge ,discomfort in nose, congested nasal mucosa and turbinates and reduced perception of smell 4.
• Patients yogya for nasya and pichu karma.

Exclusion Criteria

• Age group below 15 & above 60 years 2 .patients with any other specific reason of nasal obstruction e.g nasal polyp, adenoids hypertrophy, tumours, carcinoma, foreign body, trauma ,any sinonasal surgeries, epistaxis etc.
• 3 .patients suffering with acute rhinitis or sinusitis.
• patients suffering with COPD,or any other severe systemic 5.pregnant women and lactating mother.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Subjective Parameter-Grading will be done considering signs & symptoms of nasanaha..	For subjective parameter 1st and 30th day

Secondary Outcome Measures

Name	Time	Method
Objective parameter..x ray pns, anterior rhinoscopy	For objective parameter on 1 and 30 thday of trial

Trial Locations

Locations (1)

Patanjali ayurveda hospital; 🇮🇳 Hardwar, UTTARANCHAL, India

Patanjali ayurveda hospital

🇮🇳Hardwar, UTTARANCHAL, India

Dr monika mishra

Principal investigator

7248520330

Mmonika851@gmail.com