ImproviNg rEnal Outcomes Following Coronary angiograPhy and/or percuTaneoUs coroNary intErventions

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMontreal Heart Institute

About this trial

The NEPTUNE triple-blind, active-placebo, adaptive, pragmatic, randomized trial aims to evaluate the effectiveness of a new intra-venous hydration strategy guided by left ventricular end-diastolic pressure (LVEDP), amount of contrast used, and baseline renal function, to prevent contrast-induced acute kidney injury (CI-AKI) and patient-oriented clinical endpoints in all-comer patients undergoing coronary angiogram and/or percutaneous coronary intervention (PCI).

Eligibility criteria

Qualifiers

Age ≥18 years;

Planned coronary angiogram and/or PCI;

Willingness to participate and to attend study visits;

Expected life expectancy ≥6 months.

Disqualifiers

Cardiogenic or non-cardiogenic shock at the time of the procedure;

Emergent procedures (e.g. STEMI);

Iodine-based contrast media received within 2 days;

Presence of Intra-Aortic Balloon Pump (IABP);

Trial design

Treatments tested in this trial

  • Personalized hydration strategy
  • Standard of care

Treatment groups

1,158 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Montreal Heart Institute

Lead sponsor

Université de Montréal

Collaborator

Canadian Institutes of Health Research (CIHR)

Collaborator