SodiUm SeleniTe Adminstration IN Cardiac Surgery (SUSTAIN CSX®-Trial).

Last updated: May 27, 2021
Sponsor: Daren K. Heyland
Overall Status: Active - Not Recruiting

Phase

3

Condition

Cardiac Disease

Heart Disease

Cardiovascular Disease

Treatment

N/A

Clinical Study ID

NCT02002247
SUSTAIN CSX
  • Ages > 18
  • All Genders

Study Summary

The aim of the investigators' research program is to investigate the effects of perioperative high dose selenium supplementation in high-risk cardiac surgical patients undergoing complicated open heart surgery. The investigators hypothesize that the therapeutic strategy tested in this randomized trial may contribute to a fewer complications, less organ injury and fewer deaths. Before the investigators conducted the large definitive trial, they conducted a pilot study to assess the feasibility of the protocol, and are rolling the pilot patients into the definitive trial.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adult patients (>/=18 years of age)
  • Scheduled to undergo elective or urgent cardiac surgery with the use ofcardiopulmonary bypass (CPB) and cardioplegic arrest that exhibit a high perioperativerisk profile as defined by the presence of one or more of the following:
  • a) Planned valve surgery combined with CABG or multiple valve replacement/repairsurgeries or combined cardiac surgical procedures involving the thoracic aorta;OR
  • b) Any cardiac surgery with a high perioperative risk profile, defined as apredicted operative mortality of ≥ 5% (EuroSCORE II).

Exclusion

Exclusion Criteria: We will exclude patients who meet any of the following criteria:

  • Isolated procedures (CABG only or valve)
  • Known hypersensitivity to sodium-selenite or to any of the constituents of thesolution.
  • Renal failure requiring dialysis at the point of screening.
  • Chronic liver disease as evidenced by a pre-operative total bilirubin >2 mg/dl or 34umol/L.
  • Disabling neuropsychiatric disorders (severe dementia, severe Alzheimer's disease,advanced Parkinson's disease).
  • Pregnancy or lactation period.
  • Simultaneous participation in another clinical trial of an experimental therapy (co-enrolment acceptable in observational studies or randomized trials of existingtherapies if permitted by both steering committees and local ethics boards).
  • Patients undergoing heart transplantation or preoperative planned LVAD insertion orcomplex congenital heart surgery.
  • Alternate contacts of investigators (required by German Regulatory Authorities).

Study Design

Total Participants: 1400
Study Start date:
January 01, 2015
Estimated Completion Date:
July 31, 2021

Study Description

Over a million patients undergo open heart surgery annually and this number is likely to accelerate as the population ages and the prevalence of diabetes and cardiovascular disease continue to increase. Unfortunately, death, organ failure, and other serious complications are all too frequent following open heart surgery, especially in some high-risk patient populations.

Selenium is a trace element that is important for many of the body's regulatory and metabolic functions especially during times of stress. International members of the study team have shown in a non-randomized study that high dose selenium supplementation was associated with improved clinical outcomes compared to a historical control group. The next step in this program of research is to conduct a randomized trial.

The aim of this research program is to investigate the effects of perioperative high dose selenium supplementation in high-risk cardiac surgical patients undergoing complicated open heart surgery. The investigators hypothesize that the therapeutic strategy tested in this randomized trial may contribute to fewer complications, less organ injury and fewer deaths.

The investigators propose to conduct a randomized, placebo-controlled, double-blind, multicentre definitive trial of 1400 patients across 20 sites in Germany and Canada, which will include the pilot study patients. An industry partner (Biosyn) will provide the product and some additional support for the European sites. Patients will be randomized to receive either a daily perioperative high-dose selenium or placebo until postoperative day 10 (maximum) or upon earlier discharge from ICU. If the hypothesis is proven true, and this simple, inexpensive nutrient reduces complications and improves recovery of patients undergoing cardiac surgery, there is the potential to dramatically change clinical practice and improve health outcomes.

Connect with a study center

  • Leuven University

    West Flanders,
    Belgium

    Site Not Available

  • Vancouver Costal Health

    Vancouver, British Columbia V5Z1M9
    Canada

    Site Not Available

  • Hamilton General Hospital

    Hamilton, Ontario
    Canada

    Site Not Available

  • London Health Sciences Centre

    London, Ontario
    Canada

    Site Not Available

  • University of Ottawa Heart Institute

    Ottawa, Ontario
    Canada

    Site Not Available

  • St. Michael's Hospital

    Toronto, Ontario
    Canada

    Site Not Available

  • Sunnybrook Health Sciences Centre

    Toronto, Ontario M4N3M5
    Canada

    Site Not Available

  • Toronto General Hospital

    Toronto, Ontario
    Canada

    Site Not Available

  • Institut de cardiologie de Montreal

    Montreal, Quebec H1C1T8
    Canada

    Site Not Available

  • McGill University Health Centre

    Montreal, Quebec
    Canada

    Site Not Available

  • Sacre Coeur

    Montreal, Quebec
    Canada

    Site Not Available

  • Sir Mortimer B. Davis Jewish General Hospital

    Montreal, Quebec H3T 1E2
    Canada

    Site Not Available

  • IUCPQ

    Quebec City, Quebec
    Canada

    Site Not Available

  • Centre de recherche CIUSSS de l'Estrie CHUS

    Sherbrooke, Quebec
    Canada

    Site Not Available

  • RWTH Aachen University Hospital

    Aachen, 52074
    Germany

    Site Not Available

  • Klinik und Poliklinik für Anästhesiologie und Operative Intensivmedizin Universitätsklinikum Bonn

    Bonn,
    Germany

    Site Not Available

  • Universitätsklinikum Frankfurt

    Frankfurt, 60590
    Germany

    Site Not Available

  • Klinik für Her- und Gefäßchirurgie Universitäts-Herzzentrum Freiburg

    Freiburg,
    Germany

    Site Not Available

  • Klinik für Herz-, Kinderherz- und Gefäßchirurgie UKGM Giessen

    Gießen,
    Germany

    Site Not Available

  • University Medical Center Schleswig-Holstein

    Kiel,
    Germany

    Site Not Available

  • Klinik und Poliklinik für Herz- und Thoraxchirurgie Uniklinik Köln

    Koln,
    Germany

    Site Not Available

  • Klinik für Anästhesiologie Universitätsmedizin Mainz

    Mainz,
    Germany

    Site Not Available

  • Klinik für Anästhesiologie Klinikum der Universität München

    München,
    Germany

    Site Not Available

  • Klinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie Universitätsmedizin Münster, Zentralklinikum

    Münster,
    Germany

    Site Not Available

  • Klinikum Oldenburg gGmbH Universitätsklinik für Anästhesiologie / Intensivmedizin / Notfallmedizin / Schmerztherapie

    Oldenburg,
    Germany

    Site Not Available

  • Klinik und Poliklinik für Anästhesiologie und Intensivtherapie Universitätsmedizin Rostock

    Rostock,
    Germany

    Site Not Available

  • Hirslanden Klinik Zurich

    Zürich, 8032
    Switzerland

    Site Not Available

  • Cleveland Clinic

    Cleveland, Ohio 44195
    United States

    Site Not Available

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