Evidence map›Paper›PMID 41711722›Full record

Trial reportESC heart failure2026

Impact of cannabidiol on myocardial recovery in patients with acute myocarditis: primary results of the ARCHER study.

Dennis M McNamara, Leslie T Cooper, Matthias G Friedrich, Yaron Arbel, Arvind Bhimaraj, Edimar Bocchi, Andrew Hamer, Artur Haddad Herdy, Mathieu Kerneis, Peter P Liu and 7 more

Abstract readRandomized Controlled TrialMulticenter StudyClinical Trial, Phase II
In one paragraph

Trial report in ESC heart failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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. Review
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

17 authors.

Dennis M McNamaraHeart and Vascular Institute, University of Pittsburgh Medical Center, 200 Lothrop Street, Pittsburgh, PA 15213, USA.ORCID 0000-0003-3215-6504
Leslie T CooperDepartment of Cardiovascular Medicine, Mayo Clinic College of Medicine and Science, Jacksonville, FL, USA.
Matthias G FriedrichDepartments of Medicine and Diagnostic Radiology, Research Institute of the McGill University Health Centre, McGill University, Montreal, QC, Canada.
Yaron ArbelSourasky Medical Center, Tel Aviv University, Tel Aviv, Israel.
Arvind BhimarajDeBakey Heart & Vascular Center, Houston, TX, USA.
Edimar BocchiInstituto do Coração Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Andrew HamerCardiol Therapeutics Inc., Oakville, ON, Canada.
Artur Haddad HerdyInstituto de Cardiologia de Santa Catarina, São José, Brazil.
Mathieu KerneisPitié Salpêtrière Hospital, Sorbonne University, Paris, France.ORCID 0000-0002-7141-5209
Peter P LiuUniversity of Ottawa Heart Institute, Ottawa, Canada.
Andrea B ParkerCardiol Therapeutics Inc., Oakville, ON, Canada.
Stuart J PocockLondon School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0003-2212-4007
Eldon R SmithCardiol Therapeutics Inc., Oakville, ON, Canada.
W H Wilson TangCleveland Clinic, Heart Vascular and Thoracic Institute, Cleveland, OH, USA.
Guillermo Torre-AmioneCardiol Therapeutics Inc., Oakville, ON, Canada.
Carsten TschöpeDeutsches Herzzentrum der Charité (DHZC), Clinict of Cardiology, Angiology and Intensive Medicine at Campus Virchow (CVK), Berlin, Germany.
ARCHER Study Group

Funding

Cardiol Therapeutics Inc.
6 · The paper itself

Abstract

introductionCannabidiol has been shown to exert significant anti-inflammatory effects and has demonstrated efficacy in murine models of autoimmune myocarditis, pericarditis, and heart failure. The ARCHER Study assessed whether a pharmaceutically produced cannabidiol formulation showed beneficial effects on cardiac magnetic resonance (CMR) endpoints known to predict prognosis in this patient population.

methodsIn a multicentre international double-blind placebo-controlled phase 2 study, we randomly assigned 109 patients within 10 days of CMR confirmed diagnosis of acute myocarditis to 12 weeks of pharmaceutically produced oral cannabidiol (active) or placebo. Dose was titrated up to 10 mg/kg of body weight twice daily. Primary endpoints were the difference in extracellular volume (ECV) and global longitudinal strain (GLS) measured by CMR at week 12. Other CMR endpoints included left-ventricular ejection fraction (LVEF), LV mass, intracellular volume (ICV), LV end-diastolic and end-systolic volumes (LVEDV, LVESV), and left-atrial end-systolic volume (LAESV).

resultsAll randomized patients (56 active/53 placebo) completed the study with no loss to follow-up. Study drug appeared safe and well tolerated. Baseline mean ECV 38.9 ± 10.9 ml, GLS -15.3 ± 3.6%, and LVEF 60.6 ± 9.9% were consistent with mild to moderate myocarditis and predominantly intact LV function. Week 12 mean ECV was 33.6 ml in the active group and 37.3 ml in the placebo group, a difference of -3.7 ml, confidence interval (CI): -7.4 to 0.1; P = .0538; GLS was -16.0% in the active group and -15.9% in the placebo group, difference of -0.1, CI: -1.2 to 1.1; P = .90. Left ventricular mass was significantly reduced in the active group at 121.1 g compared to placebo 130.3 g, a difference of -9.2, CI: -16.4 to -2.1; P = .0117. In terms of remodelling, LAESV was significantly reduced in the active group (-8.1 ml; P = .0376) while the reduction in LVEDV failed to reach significance (-7.4 ml; P = .098).

conclusionIn mild-to-moderate acute myocarditis, treatment with pharmaceutically manufactured cannabidiol was not associated with a statistically significant change in myocardial ECV or GLS, although a trend towards reduction in ECV was observed. In addition, improvement in other potential markers of myocardial recovery, including a significant reduction in LV mass, was seen in the active treatment group. Further investigation of the therapeutic potential of this therapy in inflammatory cardiac conditions is warranted.

Indexed as

CannabidiolMyocarditisMyocardiumRecovery of FunctionStroke VolumeVentricular Function, LeftAcute DiseaseAdultDose-Response Relationship, DrugDouble-Blind MethodFemaleFollow-Up StudiesGlobal Longitudinal StrainHumansMagnetic Resonance Imaging, CineMaleCannabidiolAnti-inflammatoryCannabidiolCMRMyocarditisRandomized trial

Identifiers

PMID41711722
PMCPMC13108291

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.