Hyperbaric Oxygen Therapy and Acute Kidney Injury
Primary Purpose
Acute Kidney Injury
Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Standard therapy
Hyperbaric Oxygen
Sponsored by
About this trial
This is an interventional treatment trial for Acute Kidney Injury
Eligibility Criteria
Inclusion Criteria:
- age > 18 years
- any cardiac surgery with cardiopulmonary bypass surgery
- ≥30% drop in kidney function within 6 hours of surgery (determined by change in creatinine from before surgery to ICU admission)
Exclusion Criteria:
- Pre-existing renal dysfunction (creatinine > 177 µmol/L)
- claustrophobia
- seizure disorder
- severe respiratory dysfunction (PaO2/fraction of inspired oxygen (FiO2) ratio <150 on 100% O2 and Peep of 10)
- active asthma or bronchospasm
- severe chronic obstructive pulmonary disease
- history of spontaneous pneumothorax or untreated pneumothorax
- congestive heart failure with left ventricular ejection fraction < 30%
- evidence of ongoing myocardial ischemia
- presence of ventricular assist device or intra-aortic balloon pump
- chronic sinusitis
- chronic/ acute otitis media or major ear drum trauma
- current treatment with bleomycin, cisplatin, doxorubicin and disulfiram
Sites / Locations
- Toronto General Hopsital University Health Network
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Standard Therapy
Standard Therapy and hyperbaric oxygen
Arm Description
Standard supportive therapies for Acute Kidney Injury (AKI), which entail optimization of hemodynamics and hemoglobin levels.
Standard therapies and treated in the hyperbaric chamber within 12 hours of surgery. There will be 4 hyperbaric oxygen treatments in 48 hours (1 every 12 hours), each treatment will last 90 minutes with 100% oxygen at 2.4 atmospheres absolute (ATA).
Outcomes
Primary Outcome Measures
Feasibility of the intervention
The proportion of patients qualified but not consented and the proportion of patients completing the study from each group.
Safety of the intervention as assessed by adverse events
Adverse events that are related to the intervention.
Secondary Outcome Measures
Full Information
NCT ID
NCT02743754
First Posted
November 30, 2015
Last Updated
May 15, 2019
Sponsor
University Health Network, Toronto
1. Study Identification
Unique Protocol Identification Number
NCT02743754
Brief Title
Hyperbaric Oxygen Therapy and Acute Kidney Injury
Official Title
Hyperbaric Oxygen Therapy for Cardiac Surgery-Associated Acute Kidney Injury: A First-in-Human Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Terminated
Study Start Date
June 10, 2016 (Actual)
Primary Completion Date
September 7, 2017 (Actual)
Study Completion Date
May 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Kidney injury is a serious complication of cardiac surgery that occurs in up to 30% of patients and increases the risk of adverse outcomes. Kidney injury initiates when oxygen supply to the kidney drops below levels that are needed for normal cellular function, causing tissue oxygen deficiency (hypoxia), activation of the inflammatory cascade, and oxidative stress. Together, these events further impair tissue oxygenation, culminating in impaired kidney function due to cellular injury and death.
There are no effective therapies for kidney injury after cardiac surgery, but there is evidence that recovery is possible if the processes of injury - i.e., impaired oxygen delivery, increased inflammatory response, and oxidative stress - are ameliorated soon after the onset of injury. Hyperbaric oxygen therapy (HBOT) - which entails the intermittent inhalation of 100% oxygen in a hyperbaric chamber at a pressure higher than one absolute atmosphere (> 760 mmHg) - has been shown to positively affect all of these processes (i.e., to improve tissue oxygenation, reduce inflammation, and reduce oxidative stress). Thus, we hypothesized that HBOT will reduce the severity of kidney injury after cardiac surgery if it is initiated soon after onset of injury. This hypothesis has not been tested in humans, but is supported by animal studies.
In this first-in-human, unblinded, controlled pilot trial, 20 adult patients who develop severe kidney injury soon after cardiac surgery will be randomized (after obtaining informed consent from the patient or surrogate) to standard-of-care or early HBOT. Severe kidney injury will be defined as a ≥30% drop in kidney function within 6 hours of surgery (as determined by change in creatinine from before surgery to Intensive Care Unit (ICU) admission). This degree of injury occurs in ~ 2% of patients and is associated with a 12-fold increase in the risk of complete kidney failure (requiring dialysis) or death. Patients will be excluded if they have any relative or absolute contraindications to HBOT (e.g., severe ventricular dysfunction, ventricular assist device, severe respiratory dysfunction, pneumothorax, bronchospasm).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard Therapy
Arm Type
Placebo Comparator
Arm Description
Standard supportive therapies for Acute Kidney Injury (AKI), which entail optimization of hemodynamics and hemoglobin levels.
Arm Title
Standard Therapy and hyperbaric oxygen
Arm Type
Active Comparator
Arm Description
Standard therapies and treated in the hyperbaric chamber within 12 hours of surgery. There will be 4 hyperbaric oxygen treatments in 48 hours (1 every 12 hours), each treatment will last 90 minutes with 100% oxygen at 2.4 atmospheres absolute (ATA).
Intervention Type
Other
Intervention Name(s)
Standard therapy
Intervention Description
The standard of care for improving oxygen delivery to the kidney. These may include blood transfusions for anemia, treatment of low blood pressure and oxygen for low blood oxygen levels.
Intervention Type
Other
Intervention Name(s)
Hyperbaric Oxygen
Intervention Description
The standard of care therapies and in addition will be treated in the hyperbaric chamber within 12 hours of surgery. There will be 4 hyperbaric oxygen treatments in 48 hours (1 every 12 hours), each treatment will last 90 minutes with 100% oxygen at 2.4 ATA.
Primary Outcome Measure Information:
Title
Feasibility of the intervention
Description
The proportion of patients qualified but not consented and the proportion of patients completing the study from each group.
Time Frame
7 days
Title
Safety of the intervention as assessed by adverse events
Description
Adverse events that are related to the intervention.
Time Frame
7 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age > 18 years
any cardiac surgery with cardiopulmonary bypass surgery
≥30% drop in kidney function within 6 hours of surgery (determined by change in creatinine from before surgery to ICU admission)
Exclusion Criteria:
Pre-existing renal dysfunction (creatinine > 177 µmol/L)
claustrophobia
seizure disorder
severe respiratory dysfunction (PaO2/fraction of inspired oxygen (FiO2) ratio <150 on 100% O2 and Peep of 10)
active asthma or bronchospasm
severe chronic obstructive pulmonary disease
history of spontaneous pneumothorax or untreated pneumothorax
congestive heart failure with left ventricular ejection fraction < 30%
evidence of ongoing myocardial ischemia
presence of ventricular assist device or intra-aortic balloon pump
chronic sinusitis
chronic/ acute otitis media or major ear drum trauma
current treatment with bleomycin, cisplatin, doxorubicin and disulfiram
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keyvan Karkouti, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toronto General Hopsital University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
Hyperbaric Oxygen Therapy and Acute Kidney Injury
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