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Published on: December 20, 2024
Efficacy and Safety of Bojungikgi-Tang for Persistent Allergic Rhinitis: A Randomized, Double-Blinded,
Su Won Lee1, Seong-Cheon Woo1, Yee Ran Lyu2
1Division of Respiratory Medicine, Department of Internal Medicine, College of Korean Medicine, Daejeon University, Daejeon 34520, Republic of Korea.
Bojungikgi-tang (BJIGT) showed potential for treating persistent allergic rhinitis (PAR), with a high dose demonstrating statistically significant symptom improvement over time. This herbal treatment was found to be safe for patients with PAR.
Area of Science:
- Integrative Medicine
- Immunology
- Pharmacology
Background:
- Conventional treatments for allergic rhinitis (AR) have limitations, including insufficient efficacy and side effects from long-term use.
- Bojungikgi-tang (BJIGT) is a traditional herbal formula with known anti-inflammatory and immunoregulatory properties.
Purpose of the Study:
- To evaluate the efficacy and safety of BJIGT in patients with persistent allergic rhinitis (PAR).
- To compare high-dose BJIGT, standard-dose BJIGT, and placebo treatments for PAR.
Main Methods:
- A randomized controlled trial involving patients with PAR assigned to high-dose BJIGT, standard-dose BJIGT, or placebo.
- A 1-week run-in period followed by a 4-week treatment phase.
- Primary outcome: change in Total Nasal Symptom Score (TNSS); secondary outcomes: quality of life, biomarkers, and safety assessments.
Main Results:
- While the BJIGT groups showed improvement in mean TNSS compared to placebo, overall statistical significance was not reached.
- An interaction effect analysis revealed statistically significant improvement in the high-dose BJIGT group versus placebo between weeks 1-2 and 3-4.
- Secondary outcomes and safety assessments showed no significant differences between BJIGT and placebo groups, with no serious adverse events reported.
Conclusions:
- BJIGT demonstrates potential as a safe treatment option for persistent allergic rhinitis.
- Further research is warranted to confirm the clinical efficacy of BJIGT for PAR, particularly high-dose regimens.
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