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NCT06793670RecruitingPhase 4

Landiolol in Mitral Valve Surgery

The Use of Landiolol in Mitral Valve sUrgery: a raNdomized, Controlled, Double-blind triAl (LUNA)

Source: ClinicalTrials.gov · Last updated 29 Dec 2025

Brief summary (registry, in English)

Chronic mitral regurgitation is the most common valvular abnormality worldwide, it occurs in 10% of the general population and its prevalence increases with age. When left untreated, it can lead to left ventricular dysfunction and cause disabling symptoms (e.g., fatigue and dyspnea), life-threatening complications (e.g., ventricular dilation, congestive heart failure) and death. Surgical correction of chronic mitral regurgitation before irreversible changes happen can be curative. Open surgical valve repair or replacement are accomplished through cardiopulmonary bypass and cardioplegic arrest. Myocardial protection is essential to guarantee an uneventful perioperative course since a not-well protected heart may lead to postoperative low-cardiac output syndrome. This occurs in 30% of high-risk patients who undergo elective cardiac surgery and is associated with 20% mortality. Cardioplegia preserves the heart during ischemic arrest by reducing its metabolic demand. The most effective cardioplegia for protection in adult cardiac surgery remains unknown and improving the protection of the heart during the ischemic arrest may potentially improve patients' postoperative outcomes. Pharmacological adjuvants to the cardioplegic solutions have been tested to mitigate the ischaemic-reperfusion injury following cardiac surgery. Ultra-short acting beta-blockers (e.g., esmolol, landiolol) decrease intraoperative myocardial metabolic demand and suppress the sympathetic response to surgical stimuli while exhibiting limited adverse effects. Few studies with limited sample size investigated the role of ultra-short acting beta-blockers in reducing perioperative ischaemia and arrhythmia after cardiac surgery. When ultra-short acting beta-blockers were administered before aortic cross-clamping and as cardioplegia adjuvant we observed a trend towards a reduction in postoperative low-cardiac output syndrome (13/98 vs 6/102; p=0.08) and in the rate of hospital re-admission at one year (26/95 v 16/96, p=0.08) with an increase in the number of patients with ejection fraction \>60% at hospital discharge (4/95 vs 11/92, p=0.06) (Zangrillo 2021). However, despite a growing body of literature exploring the role of ultra-short acting beta-blockers in enhancing myocardial protection during on-pump cardiac surgery, further high-quality evidence is needed before this practice can be established as standard routine care. Hence, we designed a randomized, placebo-controlled trial involving 1500 patients undergoing open mitral valve surgery to assess the effect of administering landiolol as cardioplegia adjuvant to reduce the occurrence of postoperative low-cardiac output syndrome. Successful results would have a significant impact on short and long-term complications.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
1500 (estimated)
First submitted
15 Jan 2025
Start date
28 Jan 2025
Primary completion date
Jun 2027
Lead sponsor
Università Vita-Salute San Raffaele
NCT number
NCT06793670

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 1500
  • From 28 Jan 2025 to the primary completion date, Jun 2027
  • 13 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of previous unusual response to beta-blockers;
  • Urgent or emergency surgery;
  • Patient already in need of mechanical circulatory support before surgery (except for IABP);
  • Pregnancy as documented by a pregnancy test performed in the last 72h before surgery;
  • Participation in a clinical trial in which an investigational drug was administered within 30 days of screening or within the 5 half-lives of the study drug, whichever is longer.

Other illness

  • Patients with hypersensitivity to the active substance or to any of the excipients;
  • Patients with severe bradycardia (less than 50 beats per minute) sick sinus syndrome, severe atrioventricular nodal conductance disorders or 2nd -3rd degree atrioventricular block and without a pacemaker;
  • Patients with cardiogenic shock, severe hypotension (MAP\<50 mmHg), decompensated heart failure or severe pulmonary hypertension (PAPs \>70 mmHg);
  • Planned use of ultra-short acting beta-blockers as intraoperative cardiac protective strategy.

Lab values

  • Patients with preoperative evidence of hypernatremia (serum sodium concentration: \> 160 mmol/L);
  • Patients with preoperative evidence of hyperchloremia (serum chloride concentration: \>115 mmol/L);

Other

  • Need for preoperative dialysis;
  • Hepatic dysfunction (defined as Child-Pugh class C);
  • Patients with non-treated phaeochromocytoma;
  • Patients with acute asthmatic attack;
  • Patients with severe, uncorrectable metabolic acidosis.
  • Refusal or inability to sign the informed consent.

Who the study is looking for

  • Older than 18 years;
  • Elective mitral valve repair or replacement surgery with planned cardiopulmonary bypass via midline sternotomy or minithoracotomy;
  • Preoperative evidence of left ventricular end-systolic diameter \>40 mm and/or left ventricular end-diastolic diameter \>60 mm and/or left ventricular ejection fraction\<60%;
  • Signed informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
AOU di Alessandria
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AlessandriaItalyRecruiting
Ospedale Cesare Arrigo
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AlessandriaItalyRecruiting
Azienda Ospedaliero Universitaria Policlinico "G. Rodolico - San Marco"
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CataniaItalyRecruiting
AOU Careggi
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FlorenceItalyRecruiting
Azienda Ospedaliero Universitaria Ospedali Riuniti di Foggia
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FoggiaItalyRecruiting
IRCCS San Martino di Genova
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GenovaItalyRecruiting
Ospedale San Raffaele
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MilanItalyRecruiting
ASST Grande Ospedale Metropolitano Niguarda
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MilanItalyRecruiting
AOU Policlinico Paolo Giaccone
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PalermoItalyRecruiting
Azienda Ospedaliero Universitaria Pisana
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PisaItalyRecruiting
AOR San Carlo
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PotenzaItalyRecruiting
Maria Cecilia Hospital S.p.A.
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RavennaItalyRecruiting
A.O. Ordine Mauriziano di Torino
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TorinoItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.