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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05708157
Other study ID # GCIRB2022-327
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 17, 2023
Est. completion date February 29, 2024

Study information

Verified date January 2023
Source Gachon University Gil Medical Center
Contact Sang Min Lee, MD, PhD
Phone 82324582713
Email sangminlee77@naver.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 240
Est. completion date February 29, 2024
Est. primary completion date February 29, 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Perinnial allergic rhinitis diagnosed by a doctor - Positive for one or more of inhalant perinneal allergen in skin prick test or serum specific IgE measurement - Age: 19 years or older - Allergic rhinitis symptoms not controlled (VAS =5) by 2-week treatment with intranasal corticosteroid Exclusion Criteria: - Compliance for one or more drugs in last 2 weeks: <80% - Use of oral corticosteroid, oral or intranasal decongestant in last 2 weeks - Initiation of allergen-specific immunotherapy in last 12 months - Seasonal allergic rhinitis - Chronic rhinosinusitis other than allergic rhinitis - Nasal polyposis - Comorbid diseases including infectious, respiratory, cardiologic, renal, gastrointestinal, endocrinologic, oncologic, hemotologic and immunologic disorders which investigators judge to affect on the study significantly. - Patients' rejection - Pregenancy or lactation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
concomitant intranasal antihistamine and corticosteroid
concomitant intranasal administration with antihistamine and corticosteroid

Locations

Country Name City State
Korea, Republic of Gachon University Gil Medical Center Incheon

Sponsors (6)

Lead Sponsor Collaborator
Gachon University Gil Medical Center Bundang Jesaeng Hospital, Chung-Ang University Gwangmyeong Hospital, Gangneung Asan Hospital, Hallym University Kangnam Sacred Heart Hospital, Hallym University Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Kim M, Ryu G, Kang SY, Kim MA, Yang SI, Lee IH, Choi GS, Kim HJ, Lee SM, Kim DK, Choi JH, Yang HJ, Kim SW; Work Group for Rhinitis, the Korean Academy of Asthma, Allergy and Clinical Immunology. Intranasal antihistamine and corticosteroid to treat allergic rhinitis: A systematic review and meta-analysis. Allergy. 2022 Nov;77(11):3436-3440. doi: 10.1111/all.15415. Epub 2022 Jul 8. No abstract available. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary TNSS total nasal symptom score 2 week
Secondary TOSS total nasal symptom score 2 week
Secondary RQLQ rhinoconjunctivitis quality-of-life questionnares 2 week
Secondary VAS visual analogue scale 2 week
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