Építés alatt – nem éles oldal
Belépés
Not yet taking people in Svédország3. fázis

GLUTAMICS III

Key facts

Where
Goteborg, Linkoping, Lund, Orebro és Uppsala, SvédországSee the 5 sites
Phase
3. fázis

Where in Svédország

  • Sahlgrenska University Hospital-Vaestra GoetalandsregionenGoteborg, SvédországToborzás még nem indult
  • Region OestergoetlandLinkoping, SvédországToborzás még nem indult
  • Region Skane Skanes UniversitetssjukhusLund, SvédországToborzás még nem indult
  • Region Oerebro LaenOrebro, SvédországToborzás még nem indult
  • Uppsala University HospitalUppsala, SvédországToborzás még nem indult

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Region Oestergoetland
Trial code
EU 2024-513575-40-01
Record updated
2026. június 4.
Original description
To establish the efficacy of intravenous glutamate infusion to prevent acute kidney injury (AKI) after coronary artery bypass surgery (CABG) among high-risk patients without diabetes.Read full original descriptionShow less

Glutamate infusion for prevention of Acute Kidney Injury in surgery for ischemic heart disease: (GLUTAMICS III = GLUTAmate for Metabolic Intervention in Coronary Surgery III)

To establish the efficacy of intravenous glutamate infusion to prevent acute kidney injury (AKI) after coronary artery bypass surgery (CABG) among high-risk patients without diabetes.

Inclusion: Adult patients without diabetes operated on heart-lung machine with CABG of at least two vessel disease or left main stenosis with or without a concomitant procedure and who either have EuroSCORE II ≥ 3.0 to which at least one cardiac or procedure related risk factor contribute or Left Ventricular Ejection Fraction ≤ 0.30 regardless of EuroSCORE II.

Exclusion: Diabetes; ambiguous food allergy known to have elicited flushing, headache, rash or asthma; age > 85 years; previous cardiac surgery; informed consent not possible because of critical condition or other reason; preoperative use of inotropic support or mechanical circulatory assist; preoperative dialysis or calculated Creatinine clearance < 30 mL/min; surgery without heart-lung machine (off-pump); concomitant Maze-procedure; surgery of ascending aorta necessitating circulatory arrest; surgery of both aortic and mitral valve.

EU CTIS 2024-513575-40-01