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Real-World study to evaluate Fluticasone Furoate - Oxymetazoline nasal spray in Allergic Rhinitis

Not Applicable
Conditions
Health Condition 1: J309- Allergic rhinitis, unspecified
Registration Number
CTRI/2022/05/042785
Lead Sponsor
Zydus Healthcare Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients with a clinical diagnosis of allergic rhinitis or any nasal condition where-in the treating physician deems the patient suitable to receive treatment with a combination of intranasal corticosteroid and nasal decongestant will be included in the study. No further inclusion or exclusion criteria were defined beyond the information given in the package insert.

Exclusion Criteria

No further inclusion or exclusion criteria were defined beyond the information given in the package insert.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
All the patients will undergo a thorough clinical evaluation as per standard / routine hospital protocol for management of allergic rhinitis at baseline and at each follow-up. Symptom scores of the last day of treatment to be compared with that of the first day of treatment for the same patient to assess for rebound congestion.Timepoint: Baseline - Day 0 <br/ ><br>First follow up - before Day 28 <br/ ><br>Second follow up - before or on Day 28
Secondary Outcome Measures
NameTimeMethod
ilTimepoint: Nil
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