Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06686862

Non-Steroidal Anti-Inflammatory Drugs in Acute Myocarditis

Prospective, randomized, multicenter, open-label clinical trial to evaluate the safety and efficacy of a 3-week ibuprofen tapering regimen compared to conventional analgesic treatment (acetaminophen) in patients with acute myocarditis and left ventricular ejection fraction ≥50%. The objective is to assess the reduction in late gadolinium enhancement on cardiac magnetic resonance imaging at 6-month follow-up.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Hospital Universitario Puerta de Hierro-Majadahonda

Majadahonda, Madrid, 28222, Spain

Location status: Recruiting

Location contact

Fernando Domínguez Rodríguez, MD, PhD

CONTACT

[email protected]

+34 91 1916000

Fernando Domínguez-Rodriguez, MD, PhD

PRINCIPAL_INVESTIGATOR

Noemí Ramos López

CONTACT

[email protected]

Pablo García-Pavía, MD, PhD

PRINCIPAL_INVESTIGATOR

About this study

The treatment for patients with uncomplicated myocarditis (left ventricular ejection fraction >50% without heart failure) is not currently well defined. Analgesic drugs are commonly used to manage pain. The use of nonsteroidal anti-inflammatory drugs (NSAIDs) among analgesics is controversial due to potential harmful effects observed in animal models. However, NSAIDs are the standard treatment for pericarditis, even when it is associated with mild myocardial involvement. In patients with acute myocarditis and normal left ventricular ejection fraction, observational studies have suggested that NSAIDs may have a beneficial effect in reducing late gadolinium enhancement (LGE) measured in cardiac magnetic resonance (CMR), an important prognostic marker in this population.

We plan to conduct a prospective, randomized, multicenter, open-label clinical trial to evaluate the safety and efficacy of NSAIDs versus conventional analgesic treatment in patients with uncomplicated acute myocarditis and left ventricular ejection fraction ≥50%.

Approximately 150 patients will be randomized 1:1 to NSAID treatment (ibuprofen tapering schedule during 3 weeks) or conventional treatment (acetaminophen or metamizole in case of allergy until pain resolution) during hospital admission. Patients will be followed for a 12-month period. Baseline CMR will be performed at initial hospitalization for acute myocarditis and at 3 and 6 months.

The primary objective is to assess the utility of ibuprofen versus conventional treatment with analgesics in acute myocarditis with preserved LVEF, in terms of reducing LGE on CMR at 6-month follow-up compared to baseline.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 years or older.
  • Patients hospitalized for confirmed acute myocarditis and left ventricular ejection fraction ventricular >50%.
  • Elevated troponin I/T (3 times above the upper limit of normal).
  • Absence of acute heart failure.
  • Absence of ischemic heart disease (ruled out by coronary angiography or coronary CT in individuals over 40 years).
  • Diagnostic criteria for myocarditis (Lake Louise, 2018 update) by cardiac magnetic resonance imaging.

Exclusion criteria

  • Kidney disease stage 3b, 4 and 5 (creatinine clearance by CKD-EPI <45 ml/min/1.73 m2).
  • Severe liver failure (Child-Pugh class C).
  • Poorly controlled pharmacological hypertension (repeatedly systolic arterial pressure >140 mmHg).
  • Diagnosis criteria for acute pericarditis.
  • Moderate or severe pericardial effusion (>10 mm in total).
  • Hypersensitivity to NSAIDs or previous use in the last 7 days.
  • Contraindication for MRI.
  • Participation in another clinical trial.
  • Pregnancy, breastfeeding, or women of childbearing age unwilling to use appropriate contraception throughout the study.
  • Any circumstance that, in the investigator's opinion, compromises participation in the clinical trial.

Treatment and study plan

Ibuprofen

Drug

Ibuprofen tapering schedule during 3 weeks. First week: Ibuprofen 600 mg every 8 hours. Second week: Ibuprofen 600 mg every 12 hours. Third week: Ibuprofen 600 mg every 24 hours.

Primary outcomes

  1. Change in late gadolinium enhancement (measured in % relative to indexed myocardial mass) compared to baseline (CMR) at admission)

    Time frame: 6 months

Secondary outcomes

  1. Change in late gadolinium enhancement (measured in % relative to indexed myocardial mass by CMR) compared to baseline at 3 months.

    Time frame: 3 months

  2. Changes in T2 mapping values (measured in milliseconds by CMR) compared to baseline at 6 months.

    Time frame: 6 months

  3. Changes in T2 mapping values (measured in milliseconds by CMR) compared to baseline at 3 months.

    Time frame: 3 months

  4. Changes in T1 mapping values (measured in milliseconds) and extracellular volume (measured in %) by CMR compared to baseline at 6 months.

    Time frame: 6 months

  5. Changes in T1 mapping values (measured in milliseconds) and extracellular volume (measured in %) by CMR compared to baseline at 3 months.

    Time frame: 3 months

  6. Compare exercise capacity using METs (metabolic equivalent) in conventional treadmill exercise test at 3 months.

    Time frame: 3 months

  7. Proportion of patients experiencing arrhythmias during treadmill exercise test at 3 months

    Time frame: 3 months

  8. Proportion of patients from each group experiencing hospitalization due to recurrent myocarditis, heart failure, severe ventricular arrhythmias, or cardiovascular death at 12 months.

    Time frame: 1 year

  9. Proportion of patients developing adverse events in each treatment group at 1 month

    Time frame: 1 month

    Adverse events: severe adverse event, grade 3-4 adverse event, adverse reaction, special interest adverse event.

Study contacts

Contact information is provided by the study sponsor or research team.

Fernando Domínguez Rodríguez, MD, PhD

CONTACT

[email protected]

+34 91 1916000

Sponsors and collaborators

Lead sponsor

Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III

Other

Collaborators

  • Puerta de Hierro University Hospital

Registry information

Official study title

Non-Steroidal Anti-Inflammatory Drugs Versus Conventional Treatment in Acute Myocarditis (INFLAMA Trial)

Acronym: INFLAMA

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Nov 13, 2024
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.