Patients with perennial allergic rhinitis whose symptoms are not controlled (visual analogue scale \[VAS\] ≥5) by 2-week treatment with intranasal corticosteroid will receive concomitant intranasal antihistamine and corticosteroid for 2 weeks. After 2-week treatment, changes in clinical parameters including VAS, total nasal symptom score (TNSS), total ocular symptom score (TOSS), rhinoconjunctivitis quality-of-life questionnaires (RQLQ) will be evaluated.
Patients with perennial allergic rhinitis whose symptoms are not controlled (visual analogue scale \[VAS\] ≥5) by 2-week treatment with intranasal corticosteroid will receive concomitant intranasal antihistamine and corticosteroid. In addition to VAS, total nasal symptom score (TNSS), total ocular symptom score (TOSS), rhinoconjunctivitis quality-of-life questionnaires (RQLQ) will be measured before treatment (baseline) and 2 week after treatment. The differences between parameters before treatment and those after 2-week treatment will be statistically analyzed using paired student t test, and p\<0.05 was considered statistically significant.
Study Type
OBSERVATIONAL
Enrollment
240
concomitant intranasal administration with antihistamine and corticosteroid
Gachon University Gil Medical Center
Incheon, South Korea
RECRUITINGTNSS
total nasal symptom score
Time frame: 2 week
TOSS
total nasal symptom score
Time frame: 2 week
RQLQ
rhinoconjunctivitis quality-of-life questionnares
Time frame: 2 week
VAS
visual analogue scale
Time frame: 2 week
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.