Evidence map›Paper›PMID 42113738›Full record

ArticlePloS one2026

Efficacy and safety of the ayurvedic formulation 'Trikatu' as an add-on to standard care in dyslipidemia: Study protocol for a randomized, double-blind, placebo-controlled trial evaluating lipid parameters, and gut microbiota.

Shruti Khanduri, Sophia Jameela, Suchanda Sahu, Sujata Devi, Bhogavalli Chandra Sekhara Rao, Kshirod Ratha, Richa Singhal, Latika Kaushik, Narayanam Srikanth, Rabinarayan Acharya

Erratum issuedAbstract readClinical Trial Protocol
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Shruti KhanduriDepartment of Ayurveda, Central Council for Research in Ayurvedic Sciences, Ministry of Ayush, New Delhi, India.
Sophia JameelaDepartment of Ayurveda, Central Council for Research in Ayurvedic Sciences, Ministry of Ayush, New Delhi, India.ORCID https://orcid.org/0000-0001-6685-3610
Suchanda SahuDepartment of Biochemistry, All India Institute of Medical Sciences, Bhubaneswar, India.
Sujata DeviDepartment of General Medicine, All India Institute of Medical Sciences, Bhubaneswar, India.
Bhogavalli Chandra Sekhara RaoDepartment of Ayurveda, Central Council for Research in Ayurvedic Sciences, Ministry of Ayush, New Delhi, India.
Kshirod RathaDepartment of Ayurveda, Central Ayurveda Research Institute, Bhubaneswar, India.
Richa SinghalScientist C, Indian Council for Medical Research-National Institute of Malaria Research, New Delhi, India.
Latika KaushikDepartment of Ayurveda, Central Council for Research in Ayurvedic Sciences, Ministry of Ayush, New Delhi, India.
Narayanam SrikanthDeputy Director General, Central Council for Research in Ayurvedic Sciences, Ministry of Ayush, New Delhi, India.
Rabinarayan AcharyaFormer Director General, Central Council for Research in Ayurvedic Sciences, Ministry of Ayush, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDyslipidemia is a leading modifiable risk factor for cardiovascular disease (CVD), with early and sustained LDL-C reduction offering significant preventive benefits. However, in low- and middle-income countries, long-term adherence to statin therapy remains alarmingly low, highlighting the need for culturally acceptable and safer adjunctive options. Trikatu, a classical Ayurvedic formulation traditionally known to enhance metabolism, may offer supportive benefits in lipid regulation. This study protocol was developed to assess the efficacy and safety of Trikatu as an add-on to standard statin therapy on lipid parameters and assess changes in gut microbiota in response to the intervention and identify microbial correlates associated with favorable lipid outcomes.

methodsThis randomized, double-blind, placebo-controlled clinical trial is being conducted at AIIMS Bhubaneswar, a tertiary care center. Total 170 participants (aged 25-60 years) with moderate to high Atherosclerotic cardiovascular disease (ASCVD) risk. Dyslipidemia, as defined by the 2019 ACC/AHA Guidelines and indicated for statin therapy, will be randomized in a 1:1 ratio to receive either Trikatu (1000 mg) or matching placebo, administered orally twice daily after food for 12 weeks along with standard statin therapy (dose/intensity as per guidelines). Primary outcome includes change in fasting serum LDL-C from baseline to 12 weeks. Secondary outcomes include changes in total cholesterol, HDL-C, triglycerides, glycemic markers (fasting glucose, HbA1c, insulin, HOMA-IR), inflammatory and metabolic markers (hs-CRP, TNF-α, IL-6, adiponectin, ghrelin, ApoA1, ApoB), resting blood pressure, and gut microbiota. The proportion of participants achieving normal cholesterol levels (<200 mg/dL) will also be assessed. Drug compliance and any adverse events will also be recorded. DISCUSSION: In individuals with moderate to high ASCVD risk, achieving and sustaining optimal lipid control remains a cornerstone of cardiovascular prevention. However, poor long-term adherence to statin therapy, especially in low-resource settings, limits real-world impact. By assessing Trikatu, effects on lipid profiles, glycemic and inflammatory markers, and gut microbiota, the study aims to explore its potential to augment cardiovascular risk reduction in a holistic and culturally acceptable manner. If proven effective and safe, Trikatu could serve as a valuable complementary strategy in dyslipidemia management. CLINICAL

trial registrationClinical Trial Registry of India (CTRI/2023/04/051942) Registered on 25/04/2023.

Indexed as

DyslipidemiasLipidsMedicine, AyurvedicAdultCardiovascular DiseasesCholesterol, LDLDouble-Blind MethodFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedRandomized Controlled Trials as TopicCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorsLipids

Identifiers

PMID42113738
PMCPMC13160312

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.