Health Condition 1: J393- Upper respiratory tract hypersensitivity reaction, site unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants eligible for this study will include individuals aged 10 50 years who are clinically diagnosed with allergic diseases of the upper respiratory tract and have an Absolute Eosinophil Count (AEC) greater than 500 cells/ L. Only patients meeting these criteria will be included for treatment with Histaminum Hydrochloricum 3X.
Exclusion criteria
Exclusion criteria: Patients will be excluded from the study if they are taking corticosteroids, antihistamines, or immunosuppressive drugs, have parasitic or autoimmune diseases, are pregnant or lactating women, or suffer from chronic systemic illnesses such as tuberculosis or malignancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effectiveness of Histaminum Hydrochloricum 3x in reducing absolute eosinophil count in patients aged 10 years to 50 years diagnosed with allergic upper respiratory tract diseases over a period of 6 weeks.Timepoint: 9 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the improvement in clinical symptoms (e.g., sneezing, nasal congestion, itching, cough) in the same patient group after administration of Histaminum Hydrochloricum 3x for 6 weeks.Timepoint: 9 months | — |
Countries
India
Contacts
C D Pachchigar College Of Homoeopathic Medicine And hospital