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Clinical Trials/CTRI/2025/09/095044
CTRI/2025/09/095044
Not yet recruiting
Phase 2

EFFICACY OF INDIVIDUALIZD HOMOEOPATHIC MEDICINE SELECTED USING COMPLETE REPERTORY IN MANAGEMENT OF ALLERGIC RHINITIS USING TNSS AND RQLQ SCALE- A RANDOMIZED SINGLE BLIND CONTROLLED TRIAL

Dr Surendra Kumar1 site in 1 country136 target enrollmentStarted: October 1, 2025Last updated:

Overview

Phase
Phase 2
Status
Not yet recruiting
Sponsor
Dr Surendra Kumar
Enrollment
136
Locations
1
Primary Endpoint
measured pre and post (Before and After) change in the TNSS total nasal symptoms score from baseline or starting of study to 12 months period

Overview

Brief Summary

A prospective study of 136 randomly selected patients of Allergic Rhinitis from the college outdoor patient department to whom, homoeopathic medicinal intervention will be done by detailed case taking, analysis & prescription to study the efficacy of homoeopathic medicines in such cases simultaneously ascertaining the efficacy of individualized Homoeopathic Medicine Selected Using Complete Repertory.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 40.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patient of 18-40 yrs.
  • old age groups, of both sexes, irrespective of their socioeconomic status.
  • Baseline TNSS score more then 05 Patient took allopathic medicine for Allergic Rhinitis.
  • Willing to provide informed consent.

Exclusion Criteria

  • Pregnant & lactating mothers will not be included.
  • Patient with other chronic disease requiring ongoing medication.
  • patients who had a history of chronic nasal or upper respiratory tract symptoms or disorders other than AR.

Outcomes

Primary Outcomes

measured pre and post (Before and After) change in the TNSS total nasal symptoms score from baseline or starting of study to 12 months period

Time Frame: 12 months period

Secondary Outcomes

  • Change in the RQLQ rhino-conjunctivitis Quality of life Questionnaires score from baseline or starting of study to 06 months of period.(•Reduce the need of conventional therapy medicine- pre and post of treatment confirming by conventional therapist.)

Investigators

Sponsor
Dr Surendra Kumar
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Surendra Kumar

Nootan Homoeopathic Medical College and Hospital

Study Sites (1)

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