Controlled Trial of Chinese Herbal Medicine to Treat Allergic Rhinitis
NCT02027194 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 298
Last updated 2015-03-13
Summary
The aim of this study is to test and compare the effectiveness between three groups - Cure-Allergic Rhinitis Syrup (CS), Yuk ping fung San (YS) and placebo groups - of adolescents (nursing students) with Allergic Rhinitis (AR) in improving their symptoms of AR, body constitution pattern and health-related quality of life.
• The hypothesis are to test the effectiveness of the CS treatment on these students' AR symptoms and quality of life at immediately, one month and two months after completion of the 4-week intervention, when compared with the YS treatment and placebo group.
1. Cure-Allergic Rhinitis Syrup (CS) group will show significantly reduction of AR symptoms over the 2-month follow-up, when compared to those in YS and placebo groups.
2. CS group will indicate a healthier body constitution pattern over the follow-up, when compared to those with YS and placebo group.
3. CS group will indicate significantly greater improvement of their quality of life over 2-month follow-up, when compared to those with YS and placebo group.
Conditions
- Allergic Rhinitis
Interventions
- DRUG
-
Cure-Allergic Rhinitis Syrup
Delivered one bottle for two weeks to the participants twice
- DRUG
-
Yu-ping-fung San
Delivered one bottle for 2-week usage to the participants twice
- DRUG
-
Delivered one bottle (wheat power with favors) for 2-week usage to the participants twice
Sponsors & Collaborators
-
The Hong Kong Polytechnic University
lead OTHER
Principal Investigators
-
Wai Tong Chien · Professor
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-06-30
- Primary Completion
- 2014-08-31
- Completion
- 2014-10-31
Countries
- Hong Kong
Study Locations
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