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Stroke Study: Operative Strategies to Reduce Cerebral Embolic Events During Coronary Artery Bypass Surgery

Primary Purpose

Stroke

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
No aortic clamping
partial occluding clamp
single cross clamp
cross clamp and partial occluding clamp
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Stroke focused on measuring Stroke, neurocognitive dysfunction, cerebral embolic events

Eligibility Criteria

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

Inclusion Criteria:

  • > 18 years
  • undergoing primary isolated coronary artery bypass surgery
  • ability to sign informed consent

Exclusion Criteria:

  • history of preoperative stroke
  • reoperative cardiac surgery
  • salvage or emergency CABG
  • known left ventricular or left atrial thrombus
  • concomitant valvular or aortic surgery

Sites / Locations

  • Emory University Hospital Midtown

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Off-pump No Clamp

Off-pump Partial Occluding Clamp

On-pump Single Cross Clamp

On-pump Double Clamp

Arm Description

Off-pump coronary artery bypass patients randomized to no clamp for proximal anastomoses.

Off-pump coronary artery bypass patients randomized to partial occluding clamp for proximal anastomoses.

On-pump coronary artery bypass patients randomized to single cross clamp for cardioplegic arrest and proximal anastomoses.

On-pump coronary artery bypass patients randomized to cross-clamp for cardioplegic arrest and partial-occluding clamp for proximal anastomoses. This strategy involves the application of two clamps.

Outcomes

Primary Outcome Measures

Cerebral embolic events measured via transcranial doppler ultrasound
Cerebral embolic events measured via transcranial doppler ultrasound

Secondary Outcome Measures

Neurocognitive dysfunction

Full Information

First Posted
December 28, 2011
Last Updated
January 20, 2017
Sponsor
Emory University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT01502683
Brief Title
Stroke Study: Operative Strategies to Reduce Cerebral Embolic Events During Coronary Artery Bypass Surgery
Official Title
Operative Strategies to Reduce Cerebral Embolic Events During Coronary Artery Bypass Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
December 2011 (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
Emory University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
One of the most devastating complications of coronary artery bypass surgery (CABG) is postoperative stroke. While there are multiple causes of stroke after CABG, particles generated during handling of the aorta is believed to account for most neurologic effects. Handling of the aorta during CABG occurs several times during the operation. One strategy to reduce aortic handling is to avoid cardiopulmonary bypass altogether by using off-pump techniques (OPCAB). Another method is to avoid the use of aortic clamps and/or to use devices that do not require aortic clamping. This study will test the hypothesis that an off-pump (OPCAB) approach and devices to perform clampless surgery will result in the least amount of aortic handling and therefore the lowest incidence and frequency of neurologic adverse events.
Detailed Description
One of the most devastating complications of coronary artery bypass surgery (CABG) is postoperative stroke. While the etiology of stroke after CABG is multifactorial, atheroemboli generated during aortic manipulation is believed to account for most cerebral embolic events. Manipulation of the aorta during CABG occurs during aortic cannulation, institution and maintenance of cardiopulmonary bypass, and during aortic clamping and unclamping with either a cross-clamp, partial-occluding clamp, or both. One operative strategy to minimize aortic manipulation is to avoid cardiopulmonary bypass altogether by using off-pump techniques (OPCAB). Another method is to avoid the use of aortic clamps and to construct proximal aortocoronary anastomoses with facilitating devices that do not require aortic clamping. The effect of these strategies on reducing cerebral embolic events and the underlying mechanism for this reduction are not well-defined. This study will test the hypothesis that an off-pump (OPCAB) approach and facilitating devices to perform clampless proximal anastomoses will result in the least amount of aortic manipulation and therefore the lowest incidence and frequency of cerebral embolic events. The approach associated with the lowest incidence of TCD-detected cerebral embolic events will also result in the lowest incidence and severity of postoperative neurocognitive decline. Transcranial Doppler ultrasonography is an established method to detect cerebral embolic signals during cardiac surgery and will be utilized to detect cerebral embolic events during the operation. After an on- or off-pump strategy is selected, patients will be subsequently randomized to one of two clamping strategies. There will be 4 groups of patients: 1) OPCAB patients randomized to no clamping (facilitating device); 2) OPCAB patients randomized to partial clamping; 3) on-pump patients randomized to double clamping; and 4) on-pump patients randomized to a single clamp strategy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, neurocognitive dysfunction, cerebral embolic events

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
193 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Off-pump No Clamp
Arm Type
Experimental
Arm Description
Off-pump coronary artery bypass patients randomized to no clamp for proximal anastomoses.
Arm Title
Off-pump Partial Occluding Clamp
Arm Type
Experimental
Arm Description
Off-pump coronary artery bypass patients randomized to partial occluding clamp for proximal anastomoses.
Arm Title
On-pump Single Cross Clamp
Arm Type
Experimental
Arm Description
On-pump coronary artery bypass patients randomized to single cross clamp for cardioplegic arrest and proximal anastomoses.
Arm Title
On-pump Double Clamp
Arm Type
Experimental
Arm Description
On-pump coronary artery bypass patients randomized to cross-clamp for cardioplegic arrest and partial-occluding clamp for proximal anastomoses. This strategy involves the application of two clamps.
Intervention Type
Procedure
Intervention Name(s)
No aortic clamping
Intervention Description
No aortic clamp used in this group. The aortic clamp is a standard cardiac surgical instrument used during cardiac operations, not a specific device used for this study.
Intervention Type
Procedure
Intervention Name(s)
partial occluding clamp
Intervention Description
The partial-occluding clamp is a standardized instrument used during coronary artery bypass surgery, it is not a specific device for this study.
Intervention Type
Procedure
Intervention Name(s)
single cross clamp
Intervention Description
The proximal anastomoses performed under single clamp is an alternative method during coronary artery bypass surgery. The single clamp essentially means that whole operation is done using the cross clamp, which is a standard instrument during cardiac operations, not a specific device for this study.
Intervention Type
Procedure
Intervention Name(s)
cross clamp and partial occluding clamp
Intervention Description
Both an aortic cross clamp and partial occluding clamp are used in this arm. Neither the cross clamp nor the partial clamp are specific devices for this study but are standard cardiac surgical instruments used during coronary artery bypass surgery and cardiac surgery.
Primary Outcome Measure Information:
Title
Cerebral embolic events measured via transcranial doppler ultrasound
Description
Cerebral embolic events measured via transcranial doppler ultrasound
Time Frame
Intraoperative cerebral embolic events
Secondary Outcome Measure Information:
Title
Neurocognitive dysfunction
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 18 years undergoing primary isolated coronary artery bypass surgery ability to sign informed consent Exclusion Criteria: history of preoperative stroke reoperative cardiac surgery salvage or emergency CABG known left ventricular or left atrial thrombus concomitant valvular or aortic surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Halkos, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory University Hospital Midtown
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30308
Country
United States

12. IPD Sharing Statement

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Stroke Study: Operative Strategies to Reduce Cerebral Embolic Events During Coronary Artery Bypass Surgery

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