Evidence map›Paper›PMID 38786427›Full record

ArticleHealthcare (Basel, Switzerland)2024

Efficacy and Safety of Bojungikgi-Tang for Persistent Allergic Rhinitis: A Randomized, Double-Blinded, Placebo-Controlled, Phase II Trial.

Su Won Lee, Seong-Cheon Woo, Yee Ran Lyu, Won-Kyung Yang, Seung-Hyung Kim, Je Hyun Kim, Si Yeon Kim, Weechang Kang, In Chul Jung, Taesoo Kim and 1 more

Abstract read
In one paragraph

Article in Healthcare (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Su Won LeeDivision of Respiratory Medicine, Department of Internal Medicine, College of Korean Medicine, Daejeon University, Daejeon 34520, Republic of Korea.ORCID 0000-0003-2473-8686
Seong-Cheon WooDivision of Respiratory Medicine, Department of Internal Medicine, College of Korean Medicine, Daejeon University, Daejeon 34520, Republic of Korea.ORCID 0000-0002-1403-5525
Yee Ran LyuKorea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Won-Kyung YangDivision of Respiratory Medicine, Department of Internal Medicine, College of Korean Medicine, Daejeon University, Daejeon 34520, Republic of Korea.ORCID 0000-0002-4493-9787
Seung-Hyung KimInstitute of Traditional Medicine and Bioscience, Daejeon University, Daejeon 34520, Republic of Korea.ORCID 0000-0002-4598-1733
Je Hyun KimClinical Trial Center, Daejeon Korean Medicine Hospital of Daejeon University, Daejeon 35235, Republic of Korea.
Si Yeon KimClinical Trial Center, Daejeon Korean Medicine Hospital of Daejeon University, Daejeon 35235, Republic of Korea.
Weechang KangDepartment of Statistics, Graduate School, Daejeon University, Daejeon 34520, Republic of Korea.
In Chul JungClinical Trial Center, Daejeon Korean Medicine Hospital of Daejeon University, Daejeon 35235, Republic of Korea.ORCID 0000-0001-7245-4990
Taesoo KimKorea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Yang Chun ParkDivision of Respiratory Medicine, Department of Internal Medicine, College of Korean Medicine, Daejeon University, Daejeon 34520, Republic of Korea.ORCID 0000-0002-5645-869X

Funding

Korea Health Industry Development Institute HI21C1339Korea Health Industry Development Institute HI23C1313Korea Institute of Oriental Medicine KSN2021330National Research Foundation of Korea NRF-2022R1A2C1007165
6 · The paper itself

Abstract

Conventional treatments for allergic rhinitis (AR) exhibit insufficiency and long-term use-related side effects. Considering the reported anti-inflammatory and immunoregulatory effects of Bojungikgi-tang (BJIGT), we aimed to assess its efficacy on persistent AR (PAR). Patients with PAR were randomly assigned in a 1:1:1 ratio into high-dose BJIGT, standard-dose BJIGT, and placebo groups, followed by 1-week run-in and 4-week treatment periods. The primary outcome included the mean change in Total Nasal Symptom Score (TNSS), with secondary outcomes encompassing the Korean Allergic Rhinitis-Specific Quality of Life Questionnaire, biomarkers, overall assessment, TNSS by AR pattern identification, and the Sasang constitution. The mean TNSS change was more improved in the BJIGT group than in the placebo group; however, no statistically significant differences were observed. Additional interaction effect analysis revealed a statistically significant improvement in the high-dose BJIGT group compared with the placebo group from weeks 1-2 to weeks 3-4. Regarding secondary outcomes, the BJIGT group exhibited similar or improved results compared with the placebo group, showing no statistically significant differences. No serious adverse effects or clinically significant changes in safety assessments were observed. Given that this study validated clinical improvement and safety, it serves as potential groundwork for pertinent future studies.

Indexed as

allergic rhinitisBojungikgi-tangBu-Zhong-Yi-Qi-Tangherbal medicineHochu-ekki-torandomized controlled trial

Identifiers

PMID38786427
PMCPMC11120927

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.