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A Clinical Study on Individualized Homoeopathic Treatment for Adults with Allergic Rhinitis

Role of individualized homoeopathic medicine in changing serum IgE level in patients of allergic rhinitis: an open-label, single-arm, pre post test clinical study in adults - nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100198
Enrollment
50
Registered
2026-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J309- Allergic rhinitis, unspecified

Interventions

Intervention1: INDIVIDUALISED HOMOEOPATHIC MEDICINE: INDIVIDUALISED HOMOEOPATHIC MEDICINES FOR 6 MONTHS BASED ON SYMPTOM SIMILARITY Control Intervention1: NIL: NIL

Sponsors

NATIONAL INSTITUTE OF HOMOEOPATHY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals diagnosed with Allergic Rhinitis, meeting the diagnostic guidelines outlined by the ARIA (Allergic Rhinitis and Its Impact on Asthma) classification. Serum IgE level greater than 100 IU/ml. Participants aged between 18 and 60 years. Individuals from all religious, caste, and socio-economic backgrounds. All genders will be considered for inclusion. Participants must be willing to provide informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Individuals diagnosed with life-threatening illnesses or uncontrolled systemic diseases that may compromise quality of life or involve any vital organ systems. Patients presenting with major complications or co-morbid conditions such as asthma or sinusitis. Individuals with a history of substance abuse or dependency. Pregnant or lactating women, as well as those planning to conceive during the study period. Patients who have received homoeopathic treatment for any chronic condition within the past one month. Individuals who are unwilling or unable to provide informed consent to participate in the study.

Design outcomes

Primary

MeasureTime frame
Serum IMMUNOGLOBULIN-E LEVEL (S. Ig-E)Timepoint: baseline to 6months

Secondary

MeasureTime frame
RQLQ RHINOCONJUNCTIVITIS QUALITY OF LIFE QUESTIONNAIRETimepoint: baseline to 6months

Countries

India

Contacts

Public ContactDR SYED AFSAR ALI

National Institute of Homeopathy

akbiswas502@gmail.com9907752932

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026