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Utility of Manual Acupressure in Allergic Rhinitis

Effect of Manual Acupressure as a Supplementary Therapy on Quality of Life in Patients of Allergic Rhinitis; a Randomised Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064405
Enrollment
80
Registered
2024-03-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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: Standard Therapy + Manual Accupressure: Intranasal corticosteroid and Oral antihistamine + Self administered manual acupressure to 5 points for 6 weeks Control Intervention1: Intranasal

Sponsors

JIPMER Intramural Research Fund
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Between the ages of 18 and 50 years 2. Clinically diagnosed as allergic rhinitis, as per ARIA guidelines and using Absolute Eosinophil Count 3. Symptom duration for more than 6 months 4. Moderate to severe allergic rhinitis (Visual Analogue Scale score of 30-70mm at baseline) 5. Symptoms severe enough to require oral antihistamines/intranasal corticosteroid usage

Exclusion criteria

Exclusion criteria: 1. Pediatric patients, less than 18 years of age 2. Patients with anatomical abnormality of nose (Deviated nasal septum, Concha bullosa etc) 3. Patients with diagnosed asthma or other chronic upper respiratory pathologies, parasitic infestations or immunological diseases 4. Pregnant and breastfeeding women 5. Patients on steroids or other immunosuppressive therapy for unrelated conditions 6. Patients using other complementary medicine systems during the study period 7. Contra-indication to cetirizine or inhalational steroid therapy

Design outcomes

Primary

MeasureTime frame
Improvement in scores of quality of life questionnaires: NRQLQ, VAS, TNSSTimepoint: Improvement in scores of quality of life questionnaires: NRQLQ, VAS, TNSS at baseline, 4 weeks and 6 weeks

Secondary

MeasureTime frame
Reduction in total serum human immunoglobulin E (IgE)Timepoint: 6 weeks

Countries

India

Contacts

Public ContactKalaiarasi Raja

JIPMER

kalaiarasi004@gmail.com9489693249

Outcome results

None listed

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