Skip to main content
Clinical Trials/CTRI/2024/12/077925
CTRI/2024/12/077925
Not yet recruiting
Not Applicable

Understanding the miasmatic background of nasal polyp and effectiveness of lemna minor 6c in its treatment a prospective single arm pre post clinical study

Bakson Homoeopathic Medical College and Hospital1 site in 1 country35 target enrollmentStarted: December 20, 2024Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Bakson Homoeopathic Medical College and Hospital
Enrollment
35
Locations
1
Primary Endpoint
Changes will be observed on SNOT20 Score Scale

Overview

Brief Summary

This is a prospective single arm pre -post study ,to see the miasmatic background of nasal polyp and effectiveness of Lemna Minor 6c in cases of Nasal Polyp by using the SNOT 20 scale .

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
16.00 Year(s) to 45.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Both male and female will be included.
  • Participants diagnosed with nasal polyp Age group of 16 -45years suffering from nasal polyp will be included Participants who will be ready to give consent and assent.
  • Rhinoscopy findings of nasal polyp.

Exclusion Criteria

  • Participants on other medication Participants with other upper respiratory tract infections (laryngitis , pharyngitis , diphtheria ,etc) Pregnant and lactating female.
  • Uncontrolled systemic or psychiatric illness Participants with other respiratory infections (chronic bronchitis, bronchial Asthma ,cystic fibrosis Participants with suffering of sinusitis.

Outcomes

Primary Outcomes

Changes will be observed on SNOT20 Score Scale

Time Frame: SNOT20 SCORE Scale will be used at baseline, every 4 weeks upto 24 weeks. | 15 month study. | 6 months enrolment | 6 months follow up | 3 months analysis | first dose at the time of case taking and subsequent doses according to follow ups.

Changes can be positive or negative or no change

Time Frame: SNOT20 SCORE Scale will be used at baseline, every 4 weeks upto 24 weeks. | 15 month study. | 6 months enrolment | 6 months follow up | 3 months analysis | first dose at the time of case taking and subsequent doses according to follow ups.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Bakson Homoeopathic Medical College and Hospital
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Annu Verma

Bakson homoeopathic medical college and hospital

Study Sites (1)

Loading locations...

Similar Trials