Rhinitis, Allergic Clinical Trial
Official title:
Mobile Phone Daily Alarm To Improve Compliance Of Intranasal Corticosteroid Among Allergic Rhinitis Patients.
Verified date | March 2021 |
Source | National University of Malaysia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized controlled trial to compare the compliance of allergic rhinitis patients towards intranasal steroids between those who use mobile daily alarm reminder and those who do not.
Status | Active, not recruiting |
Enrollment | 207 |
Est. completion date | June 22, 2022 |
Est. primary completion date | June 22, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years to 66 Years |
Eligibility | Inclusion Criteria: - • Patients aged 15 years old to 60 years old with persistent AR - Positive SPT towards DF, DP, BT, cockroach, Aspergillus, Cat fur - Own and able to operate functioning mobile smartphone with built in alarm - Able to understand simple instructions - Patients who can read in English and Malay - Newly diagnosed AR or previous patients who only take intranasal corticosteroid less than 4 times per week Exclusion Criteria: - • Patients on immunotherapy - Patients with mild intermittent AR - Pregnant patients - Patient with psychiatric illness - Patients with gross anatomical obstruction (severe DNS, gross polyposis, nasal tumour) - Chronic rhinosinusitis(CRS) with or without nasal polyposis - Patients who have adverse reaction towards INCS - Patients with severe hearing loss |
Country | Name | City | State |
---|---|---|---|
Malaysia | Universiti Kebangsaan Malaysia Medical center | Kuala Lumpur | WP Kuala Lumpur |
Lead Sponsor | Collaborator |
---|---|
National University of Malaysia | Glenmark Pharmaceuticals S.A. |
Malaysia,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Compliance | Compliance was taken as 2/3rd use of INCS (20 days out of 30) = 20 x 0.38 = 7.6 g reduced weight. | 30 days |
Status | Clinical Trial | Phase | |
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