Preoperative Intravenous Ferric Carboxymaltose and Placebo in the Treatment of Patients Undergoing Cardiac Surgery (PREFER-CABG)
Primary Purpose
Coronary Artery Disease, Postoperative Complications, Aortic Valve Stenosis
Status
Recruiting
Phase
Phase 4
Locations
Finland
Study Type
Interventional
Intervention
Ferric carboxymaltose
Physiological saline
Sponsored by
About this trial
This is an interventional prevention trial for Coronary Artery Disease focused on measuring CABG, cardiac surgery, blood transfusion, intravenous iron, postoperative infection
Eligibility Criteria
Inclusion criteria:
- Patients presenting with cardiac disease requiring surgical operation
Open heart surgery is considered the best appropriate treatment strategy according to the current guidelines.
- significant three vessel disease
- left main disease ± single, two or three vessel disease
- two-vessel disease with proximal LAD stenosis
- coronary artery disease requiring revascularization not amenable to percutaneous coronary intervention
- Aortic valve disease requiring aortic valve surgery
- Mitral valve disease requiring surgical mitral surgery
- Combined surgery for revascularization and valve disease
- surgery of ascending aorta
- Have provided signed written informed consent
Exclusion Criteria:
- Age < 35 years
- Patients requiring , emergency or salvage cardiac surgical operation
- Participation in another clinical study or treatment with another investigational product 30 days prior to randomization
- Moribund patient not expected to survive surgery 12 months after surgery
- Active malignant disease with a short life expectancy, not eligible for surgery
- Hemoglobin levels > 155 g/dL for women and >167 g/dl for men (upper reference limits for TYKSlab)
- Ferritin levels >150 ug/l for women and >400 ug/l for men.
- Renal dialysis therapy for chronic renal failure or severe preoperative renal impairment (eGFR<30ml/min).
- Study treatment can't be infused during the required time window: minimum 48 hours and maximum 21 days before the operation.
- Ongoing oral or parenteral iron medication at the time of randomization
- Iron or haemoglobin metabolism or synthesis disorders
- Primary or secondary hemochromatosis (in males and postmenopausal females, a serum ferritin value of over 300 ng/mL (670 pmol/L); and in premenopausal females, a serum ferritin value of over 150[17] or 200[18] ng/mL (330 or 440 pmol/L) indicates iron overload).
- Porphyria cutanea tarda.
- Liver failure (Child-Pugh class B or C).
- Pregnancy.
- Body weight less than 50kg.
- Ongoing antibiotic treatment other than prophylactic urine tract infection antibiotics.
Sites / Locations
- Turku University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Ferric carboxymaltose
Placebo
Arm Description
Preoperative 1000 mg intravenous single dose as 30 minute infusion
Preoperative 100 ml saline as 30 minute infusion
Outcomes
Primary Outcome Measures
Incidence of allogeneic blood transfusion and/or nosocomial infection
Composite of transfused red blood cell units and/or nosocomial infection
Secondary Outcome Measures
Mortality
All-cause mortality
ICU/CCU days
Days in the ICU (intensive care unit) and/or CCU (cardiac care unit)
Perioperative myocardial infarction
MI (myocardial infarction) assessed by postoperative CK-Mbm or Troponin t levels
Length of stay
Days in hospital
Days on vasoactive drugs
Days on vasopressors (e.g. epinephrine, norepinephrine, milrinone etc.)
Ventilator free days
Days not on ventilator (intubated or non-invasive ventilation)
AKI (acute kidney injury)
Rate of acute renal failure
New onset atrial fibrillation (AF) or flutter
New AF or flutter (i.e. patient without previous history of AF/flutter) assessed from ECG-telemetry during index hospitalization or ECG-verified AF/flutter after discharge
Acute heart failure
Acute congestive heart failure (diagnosed by a clinician) requiring hospitalization
Worsening heart failure
Worsening to NYHA -class (New York Heart Association) III/IV or readmission for heart failure
Health related quality of life
Assessed with self-reporting questionnaire
Full Information
NCT ID
NCT03574311
First Posted
June 14, 2018
Last Updated
April 19, 2021
Sponsor
Turku University Hospital
Collaborators
Vifor Pharma
1. Study Identification
Unique Protocol Identification Number
NCT03574311
Brief Title
Preoperative Intravenous Ferric Carboxymaltose and Placebo in the Treatment of Patients Undergoing Cardiac Surgery
Acronym
PREFER-CABG
Official Title
A Phase IV Double-blind, Randomised, Parallel Group Comparison of the Efficacy and Safety of Preoperative Intravenous Ferric Carboxymaltose and Placebo in the Treatment of Patients Undergoing Elective or Urgent Cardiac Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Recruiting
Study Start Date
October 2, 2018 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Turku University Hospital
Collaborators
Vifor Pharma
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluates the efficacy and safety of single dose preoperative ferric carboxymaltose in the prevention of postoperative infections and blood transfusions in patients scheduled for cardiac surgery. Half of the patients will receive ferric carboxymaltose and half of the patients physiological saline solution as placebo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Postoperative Complications, Aortic Valve Stenosis, Mitral Valve Disease, Aortic Aneurysm, Thoracic
Keywords
CABG, cardiac surgery, blood transfusion, intravenous iron, postoperative infection
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled 1:1
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Double blinding, study drug administration by separate staff blinded from participant and investigators
Allocation
Randomized
Enrollment
210 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ferric carboxymaltose
Arm Type
Experimental
Arm Description
Preoperative 1000 mg intravenous single dose as 30 minute infusion
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Preoperative 100 ml saline as 30 minute infusion
Intervention Type
Drug
Intervention Name(s)
Ferric carboxymaltose
Intervention Description
A single dose of drug or placebo is administered preoperatively to participants
Intervention Type
Other
Intervention Name(s)
Physiological saline
Intervention Description
Single infusion 100 ml physiological saline infusion preoperatively
Primary Outcome Measure Information:
Title
Incidence of allogeneic blood transfusion and/or nosocomial infection
Description
Composite of transfused red blood cell units and/or nosocomial infection
Time Frame
0-90 days
Secondary Outcome Measure Information:
Title
Mortality
Description
All-cause mortality
Time Frame
0-90 days
Title
ICU/CCU days
Description
Days in the ICU (intensive care unit) and/or CCU (cardiac care unit)
Time Frame
0-90 days
Title
Perioperative myocardial infarction
Description
MI (myocardial infarction) assessed by postoperative CK-Mbm or Troponin t levels
Time Frame
3 days
Title
Length of stay
Description
Days in hospital
Time Frame
0-90 days
Title
Days on vasoactive drugs
Description
Days on vasopressors (e.g. epinephrine, norepinephrine, milrinone etc.)
Time Frame
0-90 days
Title
Ventilator free days
Description
Days not on ventilator (intubated or non-invasive ventilation)
Time Frame
0-90 days
Title
AKI (acute kidney injury)
Description
Rate of acute renal failure
Time Frame
0-90 days
Title
New onset atrial fibrillation (AF) or flutter
Description
New AF or flutter (i.e. patient without previous history of AF/flutter) assessed from ECG-telemetry during index hospitalization or ECG-verified AF/flutter after discharge
Time Frame
0-90 days
Title
Acute heart failure
Description
Acute congestive heart failure (diagnosed by a clinician) requiring hospitalization
Time Frame
90 days
Title
Worsening heart failure
Description
Worsening to NYHA -class (New York Heart Association) III/IV or readmission for heart failure
Time Frame
0-90 days
Title
Health related quality of life
Description
Assessed with self-reporting questionnaire
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Patients presenting with cardiac disease requiring surgical operation
Open heart surgery is considered the best appropriate treatment strategy according to the current guidelines.
significant three vessel disease
left main disease ± single, two or three vessel disease
two-vessel disease with proximal LAD stenosis
coronary artery disease requiring revascularization not amenable to percutaneous coronary intervention
Aortic valve disease requiring aortic valve surgery
Mitral valve disease requiring surgical mitral surgery
Combined surgery for revascularization and valve disease
surgery of ascending aorta
Have provided signed written informed consent
Exclusion Criteria:
Age < 35 years
Patients requiring , emergency or salvage cardiac surgical operation
Participation in another clinical study or treatment with another investigational product 30 days prior to randomization
Moribund patient not expected to survive surgery 12 months after surgery
Active malignant disease with a short life expectancy, not eligible for surgery
Hemoglobin levels > 155 g/dL for women and >167 g/dl for men (upper reference limits for TYKSlab)
Ferritin levels >150 ug/l for women and >400 ug/l for men.
Renal dialysis therapy for chronic renal failure or severe preoperative renal impairment (eGFR<30ml/min).
Study treatment can't be infused during the required time window: minimum 48 hours and maximum 21 days before the operation.
Ongoing oral or parenteral iron medication at the time of randomization
Iron or haemoglobin metabolism or synthesis disorders
Primary or secondary hemochromatosis (in males and postmenopausal females, a serum ferritin value of over 300 ng/mL (670 pmol/L); and in premenopausal females, a serum ferritin value of over 150[17] or 200[18] ng/mL (330 or 440 pmol/L) indicates iron overload).
Porphyria cutanea tarda.
Liver failure (Child-Pugh class B or C).
Pregnancy.
Body weight less than 50kg.
Ongoing antibiotic treatment other than prophylactic urine tract infection antibiotics.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jarmo M Gunn, adj. professor
Phone
+35823130000
Email
jarmo.gunn@tyks.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Tuija Vasankari, RN
Phone
+35823130000
Facility Information:
Facility Name
Turku University Hospital
City
Turku
ZIP/Postal Code
20521
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jarmo M Gunn, PhD
Phone
+35823130548
Email
jarmo.gunn@tyks.fi
First Name & Middle Initial & Last Name & Degree
Tuija Vasankari, RN
Phone
+35823130000
Email
tuija.vasankari@tyks.fi
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Preoperative Intravenous Ferric Carboxymaltose and Placebo in the Treatment of Patients Undergoing Cardiac Surgery
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