Skip to main content
Clinical Trials/CTRI/2024/08/072609
CTRI/2024/08/072609RecruitingPhase 2/3

Clinical Study To Evaluate The Efficacy Of Marsha Nasya With Shadbindu Taila On Nasal Flora In Pratishyaya(Rhinitis)

Sri Dharmasthala Manjunatheshwara college of Ayurveda and Hospital1 site in 1 country30 target enrollmentStarted: August 27, 2024Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
The subjective and Objective parameters of baseline data to post medication data compared for assessment of the final results.

Study Overview

Brief Summary

It’s important to note that the relationship between nasal flora and rhinitis is complex and not fully understood. Research in this area continues to explore how changes in nasal flora may contribute to the development or exacerbation of rhinitis and how restoring microbial balance might influence treatment outcomes. So , treatment like Marsha Nasya with Shadbindu Taila is being studied for their potential to modulate nasal flora and alleviate rhinitis symptoms

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
20.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Participants fulfilling the diagnostic criteria 20-60 years of either gender.
  • Participants who are ready to sign the informed consent.
  • Participants who are diagnosed with pratishyaya and are fit for Nasya.

Exclusion Criteria

  • Pregnancy and lactating women History of nasal polyp, Deviated nasal septum, any chronic respiratory illness.
  • History of antibiotics intake in last three months Diagnosed cases of systemic disorders like chronic heart disease, chronic renal failure and chronic liver disease.
  • Diagnosed cases of HIV, HBsAg, Carcinoma and Tuberculosis.

Outcomes

Primary Outcomes

The subjective and Objective parameters of baseline data to post medication data compared for assessment of the final results.

Time Frame: 1 week

The collected swab samples will be analysed for the number and variety of microorganisms.

Time Frame: 1 week

Secondary Outcomes

  • To assess the improvement in quality of life(improvement in quality of life will be assessed for)

Investigators

Sponsor
Sri Dharmasthala Manjunatheshwara college of Ayurveda and Hospital
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Ankita Das

Sri Dharmasthala Manjunatheshwara College of Ayurveda & Hospital, Hassan

Study Sites (1)

Loading locations...

Similar Trials