Pre-operative Short-term Administration of a Formula Diet Containing a Non-milk-derived Protein Source for Prevention of Acute Kidney Injury After Cardiac Surgery (UNICORN)
Primary Purpose
Acute Renal Failure, Acute Kidney Injury
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Non-milked derived protein source formula diet
Sponsored by
About this trial
This is an interventional prevention trial for Acute Renal Failure focused on measuring Acute kidney injury, Acute renal failure, Diet, Cardiothoracic surgery, Change of protein source
Eligibility Criteria
Inclusion Criteria:
- Men and women ≥50 years of age
- Caucasian ethnicity
- Scheduled cardiac surgery with use of the heart-lung machine with a lead time of at least 9 days
- Written informed consent
Exclusion Criteria:
- Chronic renal replacement therapy
- Status post kidney transplantation
- Vegetarian lifestyle
- BMI <18.5 kg/m2
- Calorie-reduced diet within the preceding 4 weeks
- Underlying wasting disease
- Uncontrolled local or systemic infection
- Contraindication for enteral nutrition
- Known allergy to or intolerance of the ingredients of the formula diets used
- Pregnancy or breastfeeding
- Absence of safe contraceptive measures or non-occurrence of menopause (in women)
- Participation in other interventional trials
- Persons who are in a dependency/employment relationship with the investigators
- Accommodation in an institution by judicial or administrative order.
Sites / Locations
- University Hospital of Cologne
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Non-milked derived protein source formula diet
Milked derived protein source formula diet
Arm Description
Formula diet based on a non-milked derived protein source
Formula diet based on a milked derived protein source
Outcomes
Primary Outcome Measures
AKI incidence within 72 hours according KDIGO classification after induction of ischemia ('cross clamping') in comparison to baseline values
The primary endpoint of the clinical trial is to investigate whether a preoperative diet with a non-milked derived protein source leads to a reduction of AKI incidence within 72 hours after surgery. AKI is defined according to KDIGO as an increase in serum creatinine of ≥0.3 mg/dl within 48 hours, or an increase of serum creatinine to ≥1.5 times baseline, which is known or presumed to have occurred within the prior 7 days, or a reduction of urine output to <0.5ml/kg/hour for more than 6 hours.
Baseline creatinine will be assessed prior to the start of the surgical procedure. The time frame for the following assessments with respect to the primary endpoint will be 72 hours from the onset of ischemia (cross-clamping). Blood samples will be obtained at 24 hours, 48 hours, and 72 hours after cross-clamping. Hourly urine output will be assessed as long as a Foley-catheter is in place.
Secondary Outcome Measures
Absolute and relative increase of serum creatinine concentration at 24 hours, 48 hours, and 72 hours after cardiac surgery ("cross clamping")
Incidence of AKI as defined by KDIGO until discharge
Occurrence of AKI according to KDIGO I, II, III
Maximum serum creatinine concentration detected postoperatively during hospitalization
Need for renal replacement treatment during hospitalization
In-hospital mortality
Length of hospital stay
Length of stay on intensive care unit (ICU)
tissue inhibitor of metalloproteinases 2 (TIMP-2) and insulin-like growth factor-binding protein 7 (IGFBP7) urine concentrations before surgery and at 4 hours and 24 hours after onset of ischemia (NephroCheck Test)
C-reactive Protein (CRP) concentration
Leukocyte count
Creatine kinase concentration
Troponin T concentration
Lactate Dehydrogenase concentration
N-terminal Pro brain natriuretic peptide (NT-ProBNP) concentration
Lactate concentration
Amino acid pattern (concentrations), Insulin concentration, insulin-like growth factors (IGF1) concentration, glucose concentration
Mortality rate at 30 and 180 days (as followed-up upon by telephone call)
Need for renal replacement therapy within 180 days after time point of surgery (as followed-up upon by telephone call)
Full Information
NCT ID
NCT03715868
First Posted
October 11, 2018
Last Updated
April 27, 2021
Sponsor
University of Cologne
Collaborators
Fresenius Kabi
1. Study Identification
Unique Protocol Identification Number
NCT03715868
Brief Title
Pre-operative Short-term Administration of a Formula Diet Containing a Non-milk-derived Protein Source for Prevention of Acute Kidney Injury After Cardiac Surgery
Acronym
UNICORN
Official Title
Pre-operative Short-term Administration of a Formula Diet Containing a Non-milk-derived Protein Source for Prevention of Acute Kidney Injury After Cardiac Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
January 15, 2019 (Actual)
Primary Completion Date
August 24, 2020 (Actual)
Study Completion Date
August 24, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cologne
Collaborators
Fresenius Kabi
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Cardiac surgery is associated with a high risk of postoperative AKI with significant morbidity and mortality. To date, no preventive or therapeutic measures exist to prevent this. According to the data from animal trials, a preoperative diet with a deficiency of milk-derived proteins may be a new preventive measure in this context.
This trial will investigate whether one week of changing the diets protein source to a non-milk-derived one prior to surgery effectively induces renal protection from post-surgery AKI in humans. Patients undergoing elective cardiac surgery are randomized into two arms. In the non-milked-derived based diet arm, patients receive an appropriate formula diet based on a protein source other than milk derived proteins. In the control arm, patients are provided with a formula diet based on milk-protein. Total amount of calories and proteins is not restricted and - due to randomization - assumed not to be significantly different between the two arms.
Detailed Description
Cardiac surgery is associated with a high risk of postoperative AKI with significant morbidity and mortality. Acute kidney injury (AKI) constitutes a significant complication in hospitalized patients with an incidence of about 30%. Depending on existing comorbidities, a mortality of up to 60% occurs in critically ill or postoperative patients with AKI. To date, no preventive or therapeutic measures exist to prevent this. According to the data from animal trials, a preoperative diet low in sulfur-containing amino acids may be a new preventive measure in this context.
This trial will investigate whether one week of changing the diets protein source to a non-milk-derived one prior to surgery effectively induces renal protection from post-surgery AKI in humans. Patients undergoing elective cardiac surgery are randomized into two arms.
In the non-milked-derived based diet arm, patients receive an appropriate formula diet based on a protein source other than milk derived proteins. The formula diet replaces the regular diet completely from day -7 until the scheduled cardiothoracic surgery. The amount of formula diet is based on individual calculations to cover the patients daily energy demand.
In the control arm, patients are provided with a formula diet based on milk-protein, accordingly. Total amount of calories and proteins is not restricted and - due to randomization - assumed not to be significantly different between the two arms.
The primary endpoint of the clinical trial is to investigate whether a preoperative diet with a deficiency of milk-derived proteins leads to a reduction of AKI incidence within 72 hours after surgery. AKI is defined according to 'Kidney Disease: Improving Global Outcomes' (KDIGO) classification as an increase in serum creatinine of ≥0.3 mg/dl within 48 hours, or an increase of serum creatinine to ≥1.5 times baseline, which is known or presumed to have occurred within the prior 7 days, or a reduction of urine output to <0.5ml/kg/hour for more than 6 hours.
Baseline creatinine will be assessed prior to the start of the surgical procedure. The time frame for the following assessments with respect to the primary endpoint will be 72 hours from the onset of ischemia (cross-clamping). Blood samples will be obtained at 24 hours, 48 hours, and 72 hours after cross-clamping. Hourly urine output will be assessed as long as a Foley-catheter is in place.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Renal Failure, Acute Kidney Injury
Keywords
Acute kidney injury, Acute renal failure, Diet, Cardiothoracic surgery, Change of protein source
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
117 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Non-milked derived protein source formula diet
Arm Type
Active Comparator
Arm Description
Formula diet based on a non-milked derived protein source
Arm Title
Milked derived protein source formula diet
Arm Type
No Intervention
Arm Description
Formula diet based on a milked derived protein source
Intervention Type
Other
Intervention Name(s)
Non-milked derived protein source formula diet
Intervention Description
Formula diet based on a non-milked derived protein source
Primary Outcome Measure Information:
Title
AKI incidence within 72 hours according KDIGO classification after induction of ischemia ('cross clamping') in comparison to baseline values
Description
The primary endpoint of the clinical trial is to investigate whether a preoperative diet with a non-milked derived protein source leads to a reduction of AKI incidence within 72 hours after surgery. AKI is defined according to KDIGO as an increase in serum creatinine of ≥0.3 mg/dl within 48 hours, or an increase of serum creatinine to ≥1.5 times baseline, which is known or presumed to have occurred within the prior 7 days, or a reduction of urine output to <0.5ml/kg/hour for more than 6 hours.
Baseline creatinine will be assessed prior to the start of the surgical procedure. The time frame for the following assessments with respect to the primary endpoint will be 72 hours from the onset of ischemia (cross-clamping). Blood samples will be obtained at 24 hours, 48 hours, and 72 hours after cross-clamping. Hourly urine output will be assessed as long as a Foley-catheter is in place.
Time Frame
Pre-operative baseline day of surgery to 72 hours after induction of ischemia
Secondary Outcome Measure Information:
Title
Absolute and relative increase of serum creatinine concentration at 24 hours, 48 hours, and 72 hours after cardiac surgery ("cross clamping")
Time Frame
Pre-operative baseline day of surgery and 24 hours, 48 hours and 72 hours after induction of ischemia
Title
Incidence of AKI as defined by KDIGO until discharge
Time Frame
Pre-operative baseline day of surgery to day of discharge, an expected average of 10 days
Title
Occurrence of AKI according to KDIGO I, II, III
Time Frame
Pre-operative baseline day of surgery to day of discharge, an expected average of 10 days
Title
Maximum serum creatinine concentration detected postoperatively during hospitalization
Time Frame
Pre-operative baseline day of surgery to day of discharge, an expected average of 10 days
Title
Need for renal replacement treatment during hospitalization
Time Frame
Patient will be followed up for the duration of hospital stay, an expected average of 10 days
Title
In-hospital mortality
Time Frame
Patient will be followed up for the duration of hospital stay, an expected average of 10 days
Title
Length of hospital stay
Time Frame
Patient will be followed up for the duration of hospital stay, an expected average of 10 days
Title
Length of stay on intensive care unit (ICU)
Time Frame
Day of admittance until day of discharge from ICU, an expected average of 2 days
Title
tissue inhibitor of metalloproteinases 2 (TIMP-2) and insulin-like growth factor-binding protein 7 (IGFBP7) urine concentrations before surgery and at 4 hours and 24 hours after onset of ischemia (NephroCheck Test)
Time Frame
Pre-operative baseline day of surgery and at 4 hours and 24 hours after induction of ischemia
Title
C-reactive Protein (CRP) concentration
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
Leukocyte count
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
Creatine kinase concentration
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
Troponin T concentration
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
Lactate Dehydrogenase concentration
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
N-terminal Pro brain natriuretic peptide (NT-ProBNP) concentration
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
Lactate concentration
Time Frame
Pre-operative day of surgery and at 24 hours after onset of ischemia
Title
Amino acid pattern (concentrations), Insulin concentration, insulin-like growth factors (IGF1) concentration, glucose concentration
Time Frame
Before start of diet and on day of admission (before surgery)
Title
Mortality rate at 30 and 180 days (as followed-up upon by telephone call)
Time Frame
Day of surgery until 180 days after time point of surgery
Title
Need for renal replacement therapy within 180 days after time point of surgery (as followed-up upon by telephone call)
Time Frame
Day of surgery until 180 days after time point of surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women ≥50 years of age
Caucasian ethnicity
Scheduled cardiac surgery with use of the heart-lung machine with a lead time of at least 9 days
Written informed consent
Exclusion Criteria:
Chronic renal replacement therapy
Status post kidney transplantation
Vegetarian lifestyle
BMI <18.5 kg/m2
Calorie-reduced diet within the preceding 4 weeks
Underlying wasting disease
Uncontrolled local or systemic infection
Contraindication for enteral nutrition
Known allergy to or intolerance of the ingredients of the formula diets used
Pregnancy or breastfeeding
Absence of safe contraceptive measures or non-occurrence of menopause (in women)
Participation in other interventional trials
Persons who are in a dependency/employment relationship with the investigators
Accommodation in an institution by judicial or administrative order.
Facility Information:
Facility Name
University Hospital of Cologne
City
Cologne
ZIP/Postal Code
50937
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
36056721
Citation
Osterholt T, Gloistein C, Todorova P, Becker I, Arenskrieger K, Melka R, Koehler FC, Faust M, Wahlers T, Benzing T, Muller RU, Grundmann F, Burst V. Preoperative Short-Term Restriction of Sulfur-Containing Amino Acid Intake for Prevention of Acute Kidney Injury After Cardiac Surgery: A Randomized, Controlled, Double-Blind, Translational Trial. J Am Heart Assoc. 2022 Sep 6;11(17):e025229. doi: 10.1161/JAHA.121.025229. Epub 2022 Sep 3.
Results Reference
derived
Learn more about this trial
Pre-operative Short-term Administration of a Formula Diet Containing a Non-milk-derived Protein Source for Prevention of Acute Kidney Injury After Cardiac Surgery
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