Protection of the Heart With Remote Ischemic Preconditioning During Heart Surgery: A Pilot Study
Primary Purpose
Remote Ischemic Preconditioning, Myocardial Protection
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Blood Pressure Cuff
Sponsored by

About this trial
This is an interventional prevention trial for Remote Ischemic Preconditioning
Eligibility Criteria
Inclusion Criteria:
- Written informed consent
- Age 18 through 80 years, inclusive
- Scheduled for heart surgery with CPB
Exclusion Criteria:
- Females of childbearing potential
- Emergency surgery
- Previous sternotomy
- Myocardial infarction within 48 hours prior to surgery
- Diabetes and/or BMI >35
- Need for Alpha2-agonists perioperatively
- Peripheral Vascular Disease
Sites / Locations
- University of Alberta
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Ischemic Preconditioned Group (rIP)
No Cuff
Arm Description
A 15-cm sterile blood pressure cuff was placed around the right thigh and connected to the inflating device, and the patient was draped obscuring the visibility of the cuff. Subsequently, the patient was randomly allocated (by opening of an envelope) to RIPC consisting of four 5-min cycles of lower limb ischemia-reperfusion induced by a tourniquet inflated to 300 mmHg
No rIP
Outcomes
Primary Outcome Measures
Myocardial Protection Against Ischemic Injury
High-sensitivity cardiac troponin T release as measured by peak hscTnT values and area-under-the-curve.
Secondary Outcome Measures
All-cause Death and Cardiovascular Long-term Outcome
Death and re-hospitalization due to any cause including heart and renal failure and new atrial fibrillation
Full Information
NCT ID
NCT00546390
First Posted
October 16, 2007
Last Updated
October 9, 2018
Sponsor
University of Alberta
1. Study Identification
Unique Protocol Identification Number
NCT00546390
Brief Title
Protection of the Heart With Remote Ischemic Preconditioning During Heart Surgery: A Pilot Study
Official Title
Protection of the Heart With Remote Ischemic Preconditioning During Heart Surgery: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
November 2007 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alberta
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to compare a treatment called remote ischemic preconditioning (rIP) to no treatment. rIP is a simple treatment that is believed to help patients recover better after heart surgery. This treatment involves applying a large blood pressure cuff to one leg. The blood pressure cuffs will be inflated for 5 minutes and then deflated for 5 minutes. This will be done 4 times in a row.
Detailed Description
Purpose:
Determine, in a pilot study, if surrogate markers of rIP can be detected in patients presenting for cardiac surgery. Specifically measure the effect of rIP on the expression profile of HSP-70, iNOS, PKC-E, p38 MAPK, PI3K, and sarcolemmal KATP
Determine if rIP influences the expression of genes known to influence substrate preference and thereby myocardial metabolism in patients undergoing heart surgery. Specifically the expression of HIF-1a, PPAR-a and AMPK
Hypothesis:
We hypothesize that rIP provides myocardial protection in patients presenting for heart surgery and that this protection is defined by a distinct gene expression profile with regards to genes involved in rIP and myocardial metabolism.
Study Design:
This proposal is for a randomized blinded pilot study on the use of rIP in patients requiring heart surgery.
Study Population:
The study will include 100 male and female patients undergoing elective heart surgery with cardiopulmonary bypass (CPB).
Randomization:
Patients will be randomized 1:1 to receive either rIP or no treatment.
Blinding Procedures:
The patient will be blinded as well as those performing the experimental analysis.
Interventions:
Remote Ischemic Preconditioning
rIP will be induced immediately following induction of anesthesia. Four 5 minute cycles of lower unilateral limb ischemia and reperfusion induced tourniquet inflation to 300 mmHg will constitute the preconditioning stimulus.
Blood sample collection/analysis
Two cardiac biopsies (50 - 200 mg) will be collected pre-bypass and post- bypass and will be analyzed for gene and protein expression.
Blood samples (4 mL) will be drawn immediately before induction of anesthesia, and at the same times as cardiac tissue samples are harvested and analyzed for gene/protein expression as well as at 1, 24, 48 and 72 hours post surgery. Troponin I and NT-ProBNP will be measured at baseline, 1, 24, 48 and 72 hours after surgery and 3 mL of blood will be collected for these tests. A total of 43 mL of blood will be collected per patient.
rIP induced changes in leukocyte gene expression will be measured at the aforementioned time points.
Other
ECG assessment on post-operative day 1, 2, and 3.
National Institute of Health stroke scale assessment will be conducted at screening and post operatively prior to hospital discharge.
Each patient will receive a telephone follow-up call at 30 days post operatively to collect adverse events and mortality data.
Experimental Methods:
qRT-PCR will be used to measure gene expression.
Immunoblotting will be used to measure protein expression
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Remote Ischemic Preconditioning, Myocardial Protection
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
57 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ischemic Preconditioned Group (rIP)
Arm Type
Experimental
Arm Description
A 15-cm sterile blood pressure cuff was placed around the right thigh and connected to the inflating device, and the patient was draped obscuring the visibility of the cuff. Subsequently, the patient was randomly allocated (by opening of an envelope) to RIPC consisting of four 5-min cycles of lower limb ischemia-reperfusion induced by a tourniquet inflated to 300 mmHg
Arm Title
No Cuff
Arm Type
No Intervention
Arm Description
No rIP
Intervention Type
Device
Intervention Name(s)
Blood Pressure Cuff
Intervention Description
The blood pressure cuff will be inflated for 5 minutes and then deflated for 5 minutes. This will be done 4 times in a row.
Primary Outcome Measure Information:
Title
Myocardial Protection Against Ischemic Injury
Description
High-sensitivity cardiac troponin T release as measured by peak hscTnT values and area-under-the-curve.
Time Frame
72 hours post operatively
Secondary Outcome Measure Information:
Title
All-cause Death and Cardiovascular Long-term Outcome
Description
Death and re-hospitalization due to any cause including heart and renal failure and new atrial fibrillation
Time Frame
6-month cardiovascular outcome
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Written informed consent
Age 18 through 80 years, inclusive
Scheduled for heart surgery with CPB
Exclusion Criteria:
Females of childbearing potential
Emergency surgery
Previous sternotomy
Myocardial infarction within 48 hours prior to surgery
Diabetes and/or BMI >35
Need for Alpha2-agonists perioperatively
Peripheral Vascular Disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barry A Finegan, MB
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alberta
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2G3
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
22222469
Citation
Lucchinetti E, Bestmann L, Feng J, Freidank H, Clanachan AS, Finegan BA, Zaugg M. Remote ischemic preconditioning applied during isoflurane inhalation provides no benefit to the myocardium of patients undergoing on-pump coronary artery bypass graft surgery: lack of synergy or evidence of antagonism in cardioprotection? Anesthesiology. 2012 Feb;116(2):296-310. doi: 10.1097/ALN.0b013e318242349a.
Results Reference
result
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/?term=Remote+Ischemic+Preconditioning+Applied+during++Isoflurane+Inhalation+Provides+No+Benefit+to+the++Myocardium+of+Patients+Undergoing+On-pump+Coronary++Artery+Bypass+Graft+Surgery
Description
PubMed link
Learn more about this trial
Protection of the Heart With Remote Ischemic Preconditioning During Heart Surgery: A Pilot Study
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