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The Effect of Dexmedetomidine Infusion on Post-operative Cognitive Function and Oxidative Stress in Cardiac Surgery

Primary Purpose

Oxidative Stress, Cognition Disorders

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Dexmedetomidine
Placebo
Sponsored by
Chulalongkorn University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Oxidative Stress

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA) physical status I-III.

Exclusion Criteria:

  • patients who were allergy to medication in the research regimen
  • preoperative left ventricular ejection fraction less than 30%
  • body mass index more than 35 kg/m2
  • preoperative mean arterial pressure less than 60 mmHg
  • preoperative heart rate less than 45/min
  • patients with impaired renal function (serum creatinine more than 1.5 mg/dl in female and 2 mg/dl in male)
  • active liver disease, and who had history of symptomatic cerebrovascular disease
  • psychiatric problem and other neurological diseases
  • patients who cannot read

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Dex group

    Placebo group

    Arm Description

    After skin incision, the Dexmedetomidine group received a loading dose of 0.5 mcg/kg of Dexmedetomidine in 20 minutes followed by a continuous IV infusion at 0.4 mcg/kg/hr until the end of operation.

    The control group received a loading dose and continuous IV infusion of normal saline at the same rate.

    Outcomes

    Primary Outcome Measures

    Numbers of Participants With Postoperative Cognitive Dysfunction (POCD)
    POCD was defined as a decline of 1 standard-deviation (1SD) of baseline score in either MoCA test or short bless test.
    Number of Participants With Postoperative Cognitive Dysfunction (POCD)
    POCD was defined as a decline of 1SD of baseline score in either MoCA test or short bless test.

    Secondary Outcome Measures

    Number of Participants With Postoperative Complications
    Neurological complication, Delirium, dysrhythmia, death
    Hospital Stay in Days
    ICU Stay in Hours

    Full Information

    First Posted
    June 1, 2016
    Last Updated
    May 21, 2018
    Sponsor
    Chulalongkorn University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03054857
    Brief Title
    The Effect of Dexmedetomidine Infusion on Post-operative Cognitive Function and Oxidative Stress in Cardiac Surgery
    Official Title
    The Effect of Dexmedetomidine Infusion on Post-operative Cognitive Function and Oxidative Stress in Patients Undergo Cardiopulmonary Bypass Machine Facilitated Elective Cardiac Surgery
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    June 2015 (undefined)
    Primary Completion Date
    December 2016 (Actual)
    Study Completion Date
    December 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Chulalongkorn University

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Objective: The aim of this study was to determine the effect of dexmedetomidine in reducing postoperative cognitive dysfunction (POCD) in cardiac surgical patients which use cardiopulmonary bypass machine (CPB). Materials and Methods: This study was double-blinded, randomized controlled trial. Patients scheduled for elective CPB facilitated cardiac surgery were randomly assigned in two groups, dexmedetomidine group (DEX) or control group. The cognitive tests (MoCA test and Short bless test) were done before the operation, 48 hours, and 7 days postoperatively. POCD was defined as a decline of 1SD of baseline score in any test. Arterial blood sample were analyzed for IL-6, IL-10, TNF-alpha and hs-CRP before induction (T0), after separation from CPB (T1), arrival at ICU (T2) and 24-hour after surgery (T3). Primary outcome was the incidence of POCD and the secondary outcomes were inflammatory response, other postoperative complications, ICU and hospital stay.
    Detailed Description
    After the patients were enrolled in the study, they were allocated into Dexmedetomidine group or control group by computer-based randomization. Patients, surgeons, anesthesiologists and researchers who performed the cognitive test were all blinded to the study groups. General anesthesia was induced with intravenously midazolam 0.1-0.2 mg/kg and fentanyl 5-10 mcg/kg or Thiopental 3-5 mg/kg or Propofol 2 mg/kg. Patients were intubated with pancuronium 1 mg/kg or rocuronium 0.6-1 mg/kg. Anesthesia was maintained with nitrous oxide in oxygen, isoflurane, fentanyl, and pancuronium or rocuronium as required. Standard monitoring was provided including an indwelling radial artery catheter and central venous catheter. Bispectral index (BIS) monitoring was applied and maintained between 40-60 through the operation. Cerebral oximetry was monitored both sides of the brain by non-invasive oximeters at forehead area and the data were recorded. After skin incision, the Dexmedetomidine group received a loading dose of 0.5 mcg/kg of Dexmedetomidine in 20 minutes followed by a continuous IV infusion at 0.4 mcg/kg/hr until the end of operation.The control group received a loading dose and continuous IV infusion of normal saline at the same rate. During the cardiopulmonary bypass, mean arterial pressure was maintained at 60-80 mmHg or 20% from baseline. If hypertension was detected, Nicardipine 0.2 mg was given intravenously. Ephedrine 6 mg or norepinephrine 4 mcg were given within 5 minutes and repeated every 5 minutes if hypotension was presented. Atropine 0.6 mg was administered for bradycardia (heart rate less than 50 beats per minute). After the operation, patients were transferred to Cardio-thoracic intensive care unit and received standard postoperative cardiac surgery care. 2 neuropsychological tests were used to evaluate patients' cognitive function; Montreal Cognitive Assessment (MoCA) and Short blessed test (SBT). These tests were chosen by King Chulalongkorn Memorial Hospital's psychiatrist based on previous studies and the statement consensus on assessment of neurobehavioral outcomes after cardiac surgery published in 1995. All patients were evaluated their cognitive function for 3 points of time, 1st time was at preoperative period (T1), 2nd time was at 48 hours postoperatively (T2) and the last one was at 7 days postoperatively or the day at discharge from the hospital (T3). POCD was defined as a decline of 1 standard deviation (1SD) of baseline score in any test. Blood samples were taken through the radial artery catheter, and sampling times were chosen as follows: before the induction of anaesthesia (T0); after separated from CPB (T1); arrival at intensive care unit (ICU) (T2); 24 hr after surgery (T3). Plasma Tissue Necrotic Factor-Alpha (TNF-α), Interleukin-6 (IL-6) and Interleukin-10 (IL-10) levels were measured by Magnetic Luminex Performance Assay. High sensitivity C-reactive protein (CRP) level were also measured by nephelometry.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Oxidative Stress, Cognition Disorders

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    100 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Dex group
    Arm Type
    Experimental
    Arm Description
    After skin incision, the Dexmedetomidine group received a loading dose of 0.5 mcg/kg of Dexmedetomidine in 20 minutes followed by a continuous IV infusion at 0.4 mcg/kg/hr until the end of operation.
    Arm Title
    Placebo group
    Arm Type
    Placebo Comparator
    Arm Description
    The control group received a loading dose and continuous IV infusion of normal saline at the same rate.
    Intervention Type
    Drug
    Intervention Name(s)
    Dexmedetomidine
    Other Intervention Name(s)
    Dex
    Intervention Description
    After skin incision, the dexmedetomidine group received a loading dose of 0.5 mcg/kg of Dexmedetomidine in 20 minutes followed by a continuous IV infusion at 0.4 mcg/kg/hr until the end of operation.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    The control group received a loading dose and continuous IV infusion of normal saline at the same volume and rate as in the dexmedetomidine group
    Primary Outcome Measure Information:
    Title
    Numbers of Participants With Postoperative Cognitive Dysfunction (POCD)
    Description
    POCD was defined as a decline of 1 standard-deviation (1SD) of baseline score in either MoCA test or short bless test.
    Time Frame
    48 hours
    Title
    Number of Participants With Postoperative Cognitive Dysfunction (POCD)
    Description
    POCD was defined as a decline of 1SD of baseline score in either MoCA test or short bless test.
    Time Frame
    7 days
    Secondary Outcome Measure Information:
    Title
    Number of Participants With Postoperative Complications
    Description
    Neurological complication, Delirium, dysrhythmia, death
    Time Frame
    7 days
    Title
    Hospital Stay in Days
    Time Frame
    30 days
    Title
    ICU Stay in Hours
    Time Frame
    7 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: American Society of Anesthesiologists (ASA) physical status I-III. Exclusion Criteria: patients who were allergy to medication in the research regimen preoperative left ventricular ejection fraction less than 30% body mass index more than 35 kg/m2 preoperative mean arterial pressure less than 60 mmHg preoperative heart rate less than 45/min patients with impaired renal function (serum creatinine more than 1.5 mg/dl in female and 2 mg/dl in male) active liver disease, and who had history of symptomatic cerebrovascular disease psychiatric problem and other neurological diseases patients who cannot read

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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