Evidence map›Paper›PMID 37187679›Full record

ArticleIntegrative medicine research2023

Beneficial effect of Gyejibokryeong-hwan on climacteric syndrome with blood stasis pattern: A randomized, double-blinded, placebo-controlled clinical pilot trial.

Kyungsun Han, Jeong-Eun Yoo, Jung-Eun Kim, Ojin Kwon, Ae-Ran Kim, Hyo-Ju Park, So-Young Jung, Mikyung Kim, Changsop Yang, Jung-Hyo Cho and 1 more

Abstract read
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Article in Integrative medicine research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kyungsun HanKorean Medicine Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Jeong-Eun YooDepartment of Obstetrics and Gynecology, College of Korean Medicine, Daejeon University, Daejeon, South Korea.
Jung-Eun KimKorean Medicine Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Ojin KwonKorean Medicine Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Ae-Ran KimClinical Research Coordinating Team, R&D Strategy Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Hyo-Ju ParkClinical Research Coordinating Team, R&D Strategy Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
So-Young JungClinical Research Coordinating Team, R&D Strategy Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Mikyung KimKorean Medicine Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Changsop YangKorean Medicine Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Jung-Hyo ChoDepartment of Internal Korean Medicine, College of Korean Medicine, Daejeon University, Daejeon, South Korea.
Jun-Hwan LeeKorean Medicine Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gyejibokryeong-hwan (GBH), a herbal mixture that is widely used for climacteric syndrome, is studied for its efficacy; however, no study evaluated the GBH indication, which is a blood-stasis pattern based on traditional Chinese medicine theory. Methods: This is a randomized, double-blinded, placebo-controlled clinical pilot trial. Fifty subjects with climacteric syndrome were recruited and randomly assigned to GBH group or placebo group. Subjects were administered GBH or placebo granules for 4 weeks followed by 4 weeks of observation period. For the primary outcome, the Menopause Rating Scale (MRS) was evaluated. For the secondary outcomes, quality of life, degrees of abdominal resistance and tenderness, blood-stasis pattern questionnaire and degree of upward movement of Results: After 4-week intervention, the mean change of total MRS score significantly decreased in the GBH group compared to the placebo group ( Conclusion: Our findings provide evidence of the feasibility of recruiting subjects with GBH indications and show that GBH may have clinical efficacy for the treatment of menopausal symptoms, especially urogenital symptoms, without any significant adverse events. Trial registration: Clinical Research Information Service (CRIS identifier: KCT0002170).

Indexed as

Climacteric syndromeGuizhifulingwanGyejibokryeong-hwanKeishibukuryoganMenopause

Identifiers

PMID37187679
PMCPMC10176163

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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.