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To assess the effect and safety of fluticasone nasal spray in allergic rhinitis

A Prospective Randomized Comparative study - To Asses the Effect and Safety of single daily dose of Fluticasone nasal spray against alternate day regimen in allergic rhinitis. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/083804
Enrollment
80
Registered
2025-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: - Health Condition 2: J00-J99- Diseases of the respiratory system

Interventions

Intervention1: Fluticasone nasal spray: Single dose daily in allergic rhinitis for 12 weeks Control Intervention1: Fluticasone Nasal spray: Single dose in alternative day in allergic rhinitis for 12

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of both genders belonging to age group 6-60 years having clinical diagnosis on the basis of history and examination of allergic rhinitis symptoms. 2. Both seasonal and perennial allergic rhinitis .

Exclusion criteria

Exclusion criteria: 1. Patients who have undergone nasal surgery and immunotherapy for the purpose of treating AR. 2. Patients with nasal diseases, like nasal polyp, ear deviated nasal septum, infectious diseases like acute rhinitis, chronic rhinitis, congestive sinusitis, atrophic rhinitis, chronic rhinosinusitis flu associated rhinitis, membrane perforations. 3.Patients with diabetes mellitus, asthma, hypertension and women who wanted to become pregnant or pregnant women or breast feeding women. 4. Patients with psychaitric illness. 5. Patients aged below the 6 years. 6. Patients aged above the 60 years.

Design outcomes

Primary

MeasureTime frame
Comparison between daily and alternate day regimen of fluticasone intranasal spray for allergic rhinitis.Timepoint: Daily and alternate day regimen of fluticasone intranasal spray for allergic rhinitis in baseline 8 weeks and 12 weeks

Secondary

MeasureTime frame
Comparison of symptom relief in both therapy regimens.Timepoint: Daily & alternate day symptom relief in both therapy regimens in baseline 8 weeks 12 weeks

Countries

India

Contacts

Public ContactDr Nikhat Anjum

Adichunchanagiri Institute of Medical Sciences

drkirannaikenthns@gmail.com9731341027

Outcome results

None listed

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