Thoracic Surgery Clinical Trial
Official title:
Continuous Cerebral Autoregulation Monitoring to Reduce Brain Injury From Cardiac Surgery
Verified date | January 2021 |
Source | Northwestern University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Neurological complications from cardiac surgery are an important source of operative mortality, prolonged hospitalization, health care expenditure, and impaired quality of life. New strategies of care are needed to avoid rising complications for the growing number of aged patients undergoing cardiac surgery. This study will evaluate novel methods for reducing brain injury during surgery from inadequate brain blood flow using techniques that could be widely employed.
Status | Completed |
Enrollment | 460 |
Est. completion date | February 28, 2020 |
Est. primary completion date | February 4, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 55 Years and older |
Eligibility | Inclusion Criteria: - Male or female patients undergoing primary or re-operative Coronary Artery Bypass Graft (CABG) and/or valvular surgery or ascending aorta surgery that requires Cardio-pulmonary bypass (CPB) who are at high risk for neurologic complications (stroke or encephalopathy) as determined by a Johns Hopkins risk score of >0.02 Exclusion Criteria: - Contraindication to MRI imaging (e.g., permanent pacemaker, cerebral arterial vascular clips) - Liver function test before surgery more than twice the upper limit of institutional normal - Pre-existing renal dysfunction defined as an estimated glomerular filtration rate of =60 mL/min, or current renal dialysis - Emergency surgery - Inability to attend outpatient visits - Visual impairment or inability to speak and read English. The patient will be excluded from further study if an adequate temporal window for Transcranial Doppler (TCD) monitoring can not be identified before surgery. |
Country | Name | City | State |
---|---|---|---|
United States | Northwestern Memorial Hospital | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Northwestern University | National Heart, Lung, and Blood Institute (NHLBI) |
United States,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite Neurological Outcome of Clinical Stroke or New Ischemic Brain Lesion on Diffusion Weighted MRI or Neurocognitive Dysfunction 4 to 6 Weeks After Surgery. | The composite neurological outcome was composed of clinical stroke, or new ischemic lesions detected on postoperative brain diffusion weighted magnetic resonance imaging(DWI), or cognitive decline from baseline to 4-6 weeks after surgery. | Up to 6 weeks post-operative | |
Secondary | Postoperative Delirium | Assessed with Confusion Assessment Method or Confusion Assessment Method-ICU along with adjudication by team of experts | Postoperative days 1-4 | |
Secondary | Multiple Inotropic Drugs>24 Hours After Surgery | Use of multiple inotropic drugs greater than 24 hours after the planned surgical procedure until discharge from the hospital. | 7 days after surgery | |
Secondary | Mechanical Lung Ventilation>24 Hours After Surgery | Subjects need for mechanical lung ventilation more than 24 hours after planned surgical procedure. | Up to 28 days after surgery. | |
Secondary | Insertion of Intra-aortic Balloon Pump | Procedural insertion of intra-aortic balloon pump within 7 days after surgical procedure | 7 days after surgery | |
Secondary | Postoperative Atrial Fibrillation | Clinical diagnosis of postoperative atrial fibrillation from date of surgical procedure to discharge from the hospital. | Up to 28 days after surgery. | |
Secondary | Sepsis | Clinical diagnosis of sepsis from time of surgical procedure to discharge from the hospital. | Up to 28 days after surgery. | |
Secondary | Acute Kidney Injury Within 7 Days After Surgery. | Subject developed acute kidney injury within 7 days after surgical procedure. Based on Kidney disease: Improving Global Outcomes (KDIGO) classification system. | 7 days after surgery | |
Secondary | New Renal Replacement Therapy | Subjects requiring new renal replacement therapy prior to discharge from hospital | Up to 28 days after surgery. | |
Secondary | Multisystem Organ Failure After Surgery | Subject diagnosis of multisystem organ failure after surgery. | Up to 28 days after surgery. | |
Secondary | Mortality | Subject death within 28 days after surgical procedure | 28 days |
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