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Clinical Trials/NCT05619653
NCT05619653
Active, not recruiting
Phase 3

Randomised Placebo Controlled Clinical Trial of Efficacy of MYOcardial Protection in Patients With Postacute inFLAMmatory Cardiac involvEment Due to COVID-19

Valentina Puentmann5 sites in 2 countries279 target enrollmentDecember 12, 2022

Overview

Phase
Phase 3
Intervention
Prednisolone
Conditions
Not specified
Sponsor
Valentina Puentmann
Enrollment
279
Locations
5
Primary Endpoint
Left ventricular ejection fraction
Status
Active, not recruiting
Last Updated
4 months ago

Overview

Brief Summary

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

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.

Registry
clinicaltrials.gov
Start Date
December 12, 2022
End Date
March 31, 2026
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Valentina Puentmann
Responsible Party
Sponsor Investigator
Principal Investigator

Valentina Puentmann

Principal Investigator

Johann Wolfgang Goethe University Hospital

Eligibility Criteria

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:
  • Known cardiac impairment with LVEF ≤44%
  • Congestive heart failure (NYHA III-IV)
  • Active heart failure treatment
  • Established ischaemic heart disease, peripheral arterial disease and/or cerebrovascular disease

Arms & Interventions

Verum

Prednisolone and Losartan

Intervention: Prednisolone

Verum

Prednisolone and Losartan

Intervention: Losartan

Placebo

Placebo 1 and Placebo 2

Intervention: Prednisolone

Placebo

Placebo 1 and Placebo 2

Intervention: Losartan

Outcomes

Primary Outcomes

Left ventricular ejection fraction

Time Frame: 16 weeks

absolute change of LVEF from baseline

Secondary Outcomes

  • Scar burden by late gadolinium enhancement (LGE)(16 weeks)
  • Cardiopulmonary exercise testing (CPET)(16 weeks)
  • Mean T1 and T2 mapping(16 Weeks)
  • LV Volume (ml/m2) and LV mass (g/m2)(16 Weeks)
  • LV strain %(16 Weeks)
  • Aortic stiffness (PWV)(16 Weeks)
  • Aortic wall imaging (LGE)(16 Weeks)
  • Average Symptom Score (Modified CCS, NYHA, MRC Dyspnea Score, LC Questionnaire (Sudre et al, NM 2020)(at all available time points compared to baseline)
  • HF and MACE Endpoints(1 year)
  • Quality of Life assessment(at all available time points compared to baseline)
  • Compliance and Tolerance of Therapy(at all available time points compared to baseline)
  • Assessment of Treatment Response(16 weeks)

Study Sites (5)

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