Evidence map›Paper›PMID 41877056›Full record

Trial reportBMC complementary medicine and therapies2026

Curcuminoid supplementation for vasomotor symptoms in postmenopausal women: a pilot, randomized, double-blind, placebo-controlled proof-of-concept trial.

Jinjutha Buntoonprayuk, Kitti Chattrakulchai, Orawin Vallibhakara, Pimpun Prasanchit, Sakda Arj-Ong Vallibhakara

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC complementary medicine and therapies, 2026. 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

5 authors.

Jinjutha BuntoonprayukDepartment of Obstetrics and Gynaecology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Kitti ChattrakulchaiMenopause Unit, Reproductive Endocrinology and Infertility Division, Department of Obstetrics and Gynaecology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. k.chattrakulchai@gmail.com.ORCID http://orcid.org/0009-0002-5887-7596
Orawin VallibhakaraMenopause Unit, Reproductive Endocrinology and Infertility Division, Department of Obstetrics and Gynaecology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0002-9980-007X
Pimpun PrasanchitReproductive Endocrinology and Infertility Division, Department of Obstetrics and Gynaecology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0003-2379-2293
Sakda Arj-Ong VallibhakaraInterdisciplinary Studies and Lifelong Education (I-Grad), Faculty of Public Health, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0001-5343-3297

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVasomotor symptoms are common during menopause and can impair quality of life. Although hormone therapy is effective, concerns about risks and adverse effects contribute to limited utilization, highlighting the need for non-hormonal options. Curcuminoids have antioxidant and anti-inflammatory properties and may improve vasomotor symptoms.

methodsThis 12-week, randomized, double-blind, placebo-controlled pilot proof-of-concept trial evaluated the preliminary efficacy of curcuminoids (1000 mg/day) versus placebo in healthy postmenopausal women (41–65 years; n = 40). The prespecified primary endpoint was the between-group difference in change in weekly hot flash frequency from baseline to Week 12. Secondary outcomes included changes in Menopause Rating Scale II (MRS II) and Menopause-Specific Quality of Life (MENQOL) scores. Safety and tolerability were assessed throughout.

resultsAll participants completed the intervention with high adherence and no serious adverse events. At Week 12 (primary endpoint), the between-group difference in change in weekly hot flash frequency from baseline was − 7.35 episodes/week (95% CI − 10.29 to − 4.41; p < 0.001), favoring curcuminoids; results were concordant using the Hodges–Lehmann estimate (− 6.00; 95% CI − 10.00 to − 4.00; p < 0.001). A significant between-group difference was also observed at Week 6. No statistically significant between-group differences were observed at Week 12 for total MENQOL or total MRS II, although the MENQOL vasomotor domain improved at Week 6 and showed supportive evidence in baseline-adjusted sensitivity analysis at Week 12.

conclusionIn this pilot proof-of-concept randomized trial, curcuminoid supplementation significantly reduced weekly hot flash frequency compared with placebo and showed a preliminary signal toward improved vasomotor-related quality of life, particularly at Week 6, with good tolerability. These preliminary, hypothesis-generating findings require confirmation in larger, adequately powered randomized trials, ideally incorporating biomarker endpoints.

trial registrationThai Clinical Trials Registry (TCTR) TCTR20241210002 (retrospectively registered).

Indexed as

CurcuminDietary SupplementsHot FlashesPostmenopauseVasomotor SystemAdultAgedDouble-Blind MethodFemaleHumansMiddle AgedPilot ProjectsProof of Concept StudyQuality of LifeCurcuminCurcuminoidsHot flashesMenopausePilot studyQuality of lifeRandomized controlled trialVasomotor symptoms

Identifiers

PMID41877056
PMCPMC13134235

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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.