MedPath

A study to assess the effectiveness of Homoeopathic medicine using Synthesis Repertory in the treatment of Allergic rhinitis.

Phase 2
Conditions
Health Condition 1: J309- Allergic rhinitis, unspecified
Registration Number
CTRI/2023/08/055974
Lead Sponsor
ational Institute of Homoeopathy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a)Patients fulfilling the diagnostic criteria of Allergic Rhinitis as per ARIA Classification.

b)Patients of age group between18-60 years of age.

c)Patients from all religions, caste, all socio-economic status and all gender.

d)Patients willing to give informed consent to participate in the study.

Exclusion Criteria

a)Patients suffering from any life-threatening illness or other uncontrolled disease affecting quality of life or any other vital organ.

b)Patients suffering from any major complications and co-morbidities such as Asthma and Sinusitis.

c)Substance abuse and/or dependence.

d)Pregnant women, lactating mothers, and women who are planning for pregnancy.

e)Patients who have taken homoeopathic medicines for any other chronic disease in the past 1 month.

f)Patients unwilling to participate in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assessment of Increase or decrease in Allergic rhinitis using E. F. Juniper Rhinoconjuctivitis Quality of Life questionnaire (RQLQ).Timepoint: Base line, 3rd month & 6th month.
Secondary Outcome Measures
NameTimeMethod
ot applicableTimepoint: Not applicable
© Copyright 2025. All Rights Reserved by MedPath