Myocardial Protection in Patients With Post-acute Inflammatory Cardiac Involvement Due to COVID-19

NCT ID: NCT05619653

Last Updated: 2025-12-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

279 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-12

Study Completion Date

2026-03-31

Brief Summary

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Long COVID or Postacute sequelae of COVID-19 infection (PASC) are increasingly recognised complications, defined by lingering symptoms, not present prior to the infection, typically persisting for more than 4 weeks. Cardiac symptoms due to post-acute inflammatory cardiac involvement affect a broad segment of people, who were previously well and may have had only mild acute illness (PASC-cardiovascular syndrome, PASC-CVS). Symptoms may be contiguous with the acute illness, however, more commonly they occur after a delay. Symptoms related to the cardiovascular system include exertional dyspnoea, exercise intolerance chest tightness, pulling or burning chest pain, and palpitations (POTS, exertional tachycardia).

Pathophysiologically, Long COVID relates to small vessel disease (endothelial dysfunction) vascular dysfunction and consequent tissue organ hypoperfusion due to ongoing immune dysregulation. Active organs with high oxygen dependency are most affected (heart, brain, kidneys, muscles, etc.). Thus, cardiac symptoms are often accompanied by manifestations of other organ systems, including fatigue, brain fog, kidney problems, myalgias, skin and joint manifestations, etc, now commonly referred to as the Long COVID or PASC syndrome.

Phenotypically, PostCOVID Heart involvement is characterised by chronic perivascular and myopericardial inflammation. We and others have shown changes using sensitive cardiac MRI imaging that relate to cardiac symptoms (Puntmann et al, Nature Medicine 2022; Puntmann et al, JAMA Cardiol 2020; Summary of studies included in 2022 ACC PostCOVID Expert Consensus Taskforce Development Statement, JACC 2022, references below).

Early intervention with immunosuppression and antiremodelling therapy may reduce symptoms and development of myocardial impairment, by minimising the disease activity and inducing disease remission. Low-dose maintenance therapy may help to maintain the disease activity at the lowest possible level. The benefits of early initiations of antiremodelling therapy to reduce symptoms of exercise intolerance are well recognised, but not commonly employed outside the classical cardiology contexts, such as heart failure or hypertension. As most patients with inflammatory heart disease only have mild or no structural abnormalities, they are left untreated (standard of care).

The aim of this study is to examine the efficacy of a combined immunosuppressive / antiremodelling therapy in patients with PASC symptoms and inflammatory cardiac involvement determined by CMR, to reduce the symptoms and inflammatory myocardial injury and thereby stop the progression to reduced LVEF, HF and death.

Detailed Description

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Patients with documented COVID-19 infection, experiencing new cardiac symptoms in the aftermath of COVID-19 infection, fulfilling predefined CMR criteria for PostCOVID myocardial involvement and no previously known or demonstrable cardiovascular disease will be randomised to 16-week treatment with Losartan/Prednisolon or placebo. All imaging is conducted with fidelity to standardised imaging protocol. All images are analysed in a dedicated core-lab to confirm eligibility for inclusion. Investigators and participants remain blinded to group allocation and imaging results.

The primary outcome is a change in LVEF from the baseline to 16 weeks measured by MRI.

Secondary outcomes include changes in clinical symptom scores, imaging parameters, CPET (VO2max), as well as outcomes after 1 years time.

Conditions

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COVID-19 Associated Cardiac Involvement Remodeling, Left Ventricle Remodeling, Vascular Left Ventricular Dysfunction Exercise Intolerance Vascular Inflammation Microvascular Angina Long COVID Myocarditis, Pericarditis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

multicentre randomised double-blind, placebo-controlled clinical trial 1:1 randomisation
Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors
Placebo

Study Groups

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Verum

Prednisolone and Losartan

Group Type ACTIVE_COMPARATOR

Prednisolone

Intervention Type DRUG

randomised double-blind, placebo-controlled clinical trial 1:1 randomisation

Losartan

Intervention Type DRUG

randomised double-blind, placebo-controlled clinical trial 1:1 randomisation

Placebo

Placebo 1 and Placebo 2

Group Type PLACEBO_COMPARATOR

Prednisolone

Intervention Type DRUG

randomised double-blind, placebo-controlled clinical trial 1:1 randomisation

Losartan

Intervention Type DRUG

randomised double-blind, placebo-controlled clinical trial 1:1 randomisation

Interventions

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Prednisolone

randomised double-blind, placebo-controlled clinical trial 1:1 randomisation

Intervention Type DRUG

Losartan

randomised double-blind, placebo-controlled clinical trial 1:1 randomisation

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients ≥ 18 years
* Patients with documented recent COVID19 infection (\>4 weeks)
* PASC Syndrome, defined by persistence or new symptoms, not present prior to the infection.
* CMR evidence of inflammatory cardiac involvement at BL by any of the following criteria:
* Increased native T1≥ 1130 ms at 3.0 Tesla (or 1030 ms at 1.5 Tesla) and/or;
* Increased native T2 ≥39.5 ms at 3.0 Tesla (or 49.5 at 1.5 Tesla) and/or
* present non-ischaemic myopericardial LGE and/or;
* LVEF ≥45 - ≤50%.
* Willingness to comply with the study procedures and study protocol

Exclusion Criteria

* Severe acute COVID illness requiring hospitalisation
* Known allergy to or intolerance of the study medications
* Symptomatic hypotension (systolic blood pressure less than 90 mm Hg), not reversible with oral hydration
* Any previous or current use of ACE inhibitors, AR Blockers
* Any previous oral prednisolone, or any other immunosuppressive or biological treatment (within prior 10 weeks)
* History or CMR evidence of pre-existing significant heart disease, including:

1. Known cardiac impairment with LVEF ≤44%
2. Congestive heart failure (NYHA III-IV)
3. Active heart failure treatment
4. Established ischaemic heart disease, peripheral arterial disease and/or cerebrovascular disease
5. Persistent or permanent atrial fibrillation or significant heart rhythm abnormalities
6. Congenital or clinically relevant valvular heart disease (moderate or severe)
7. Specific cardiomyopathy (hypertrophic, hypertensive heart disease, amyloidosis, previous myocarditis, non-ischaemic dilated cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, non-compaction cardiomyopathy, etc).
* Known significant concomitant diseases that are likely to interfere with the evaluation of the patient's safety and of the study outcome (e.g. diabetes, lung or hepatic disease, epilepsy, psychiatric disorders, renal disease with a current estimated GFR \<30 mL/min/1.73 m² using MDRD formula, chronic systemic infection or immunocompromise)
* Exceeding scanner bore and table-holding capacity: Weight \>125 kg, BMI \> 35 kg/m2
* Contraindications to contrast-enhanced CMR imaging, e.g.

1. MR-unsafe implantable device
2. known allergy to gadolinium-based contrast agent (CBGA)
* For female participants:

1. Pregnant or breastfeeding women
2. Persons of childbearing potential not willing to use effective contraception (defined as PEARL index \<1 - e.g. contraceptive pill, IUD)
* Known alcohol, drug or chemical abuse
* Patients currently participating in an investigational study or for whom participation is planned.
* Unable to provide written informed consent

Patients with CMR evidence of structural heart disease or incidental heart rhythm abnormalities will be advised to see their own doctor for further investigation.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bayer

INDUSTRY

Sponsor Role collaborator

Alcedis GmbH

INDUSTRY

Sponsor Role collaborator

Valentina Puentmann

OTHER

Sponsor Role lead

Responsible Party

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Valentina Puentmann

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Valentina Puntmann, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Goethe University Frankfurt

Eike Nagel, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Goethe University Frankfurt

Locations

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University Medical Centre Vienna

Vienna, , Austria

Site Status

Institute for experimental and translational cardiovascular imaging

Frankfurt am Main, Hesse, Germany

Site Status

University Hospital Greifswald

Greifswald, , Germany

Site Status

University Hospital Schleswig-Holstein, Campus KIEL

Kiel, , Germany

Site Status

University Hospital Ulm

Ulm, , Germany

Site Status

Countries

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Austria Germany

References

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Puntmann VO, Martin S, Shchendrygina A, Hoffmann J, Ka MM, Giokoglu E, Vanchin B, Holm N, Karyou A, Laux GS, Arendt C, De Leuw P, Zacharowski K, Khodamoradi Y, Vehreschild MJGT, Rohde G, Zeiher AM, Vogl TJ, Schwenke C, Nagel E. Long-term cardiac pathology in individuals with mild initial COVID-19 illness. Nat Med. 2022 Oct;28(10):2117-2123. doi: 10.1038/s41591-022-02000-0. Epub 2022 Sep 5.

Reference Type BACKGROUND
PMID: 36064600 (View on PubMed)

Writing Committee; Gluckman TJ, Bhave NM, Allen LA, Chung EH, Spatz ES, Ammirati E, Baggish AL, Bozkurt B, Cornwell WK 3rd, Harmon KG, Kim JH, Lala A, Levine BD, Martinez MW, Onuma O, Phelan D, Puntmann VO, Rajpal S, Taub PR, Verma AK. 2022 ACC Expert Consensus Decision Pathway on Cardiovascular Sequelae of COVID-19 in Adults: Myocarditis and Other Myocardial Involvement, Post-Acute Sequelae of SARS-CoV-2 Infection, and Return to Play: A Report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2022 May 3;79(17):1717-1756. doi: 10.1016/j.jacc.2022.02.003. Epub 2022 Mar 16. No abstract available.

Reference Type BACKGROUND
PMID: 35307156 (View on PubMed)

Puntmann VO, Carerj ML, Wieters I, Fahim M, Arendt C, Hoffmann J, Shchendrygina A, Escher F, Vasa-Nicotera M, Zeiher AM, Vehreschild M, Nagel E. Outcomes of Cardiovascular Magnetic Resonance Imaging in Patients Recently Recovered From Coronavirus Disease 2019 (COVID-19). JAMA Cardiol. 2020 Nov 1;5(11):1265-1273. doi: 10.1001/jamacardio.2020.3557.

Reference Type BACKGROUND
PMID: 32730619 (View on PubMed)

Puntmann VO, Beitzke D, Kammerlander A, Voges I, Gabbert DD, Doerr M, Chamling B, Bozkurt B, Kaski JC, Spatz E, Herrmann E, Rohde G, DeLeuw P, Taylor L, Windemuth-Kieselbach C, Harz C, Santiuste M, Schoeckel L, Hirayama J, Taylor PC, Berry C, Nagel E. Design and rationale of MYOFLAME-19 randomised controlled trial: MYOcardial protection to reduce post-COVID inFLAMmatory heart disease using cardiovascular magnetic resonance Endpoints. J Cardiovasc Magn Reson. 2025 Summer;27(1):101121. doi: 10.1016/j.jocmr.2024.101121. Epub 2024 Oct 29.

Reference Type BACKGROUND
PMID: 39481808 (View on PubMed)

Related Links

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Other Identifiers

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2022-001682-12

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

MYOFLAME-19

Identifier Type: -

Identifier Source: org_study_id

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