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Remote Ischemic Conditioning to Attenuate Myocardial Death and Improve Operative Outcome. (RICARDO)

Primary Purpose

Coronary Artery Bypass, Myocardial Reperfusion Injur, Ischemic Preconditioning, Myocardial

Status
Unknown status
Phase
Phase 2
Locations
Poland
Study Type
Interventional
Intervention
Remote Ischemic Preconditioning with Postconditioning
Sham RIPC procedure
Sponsored by
Medinet Heart Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Bypass focused on measuring myocardial protection, remote ischemic preconditioning, remote ischemic postconditioning, cardiac surgery

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients qualified to coronary artery bypass grafting according to ESC/EACTS Guidelines of myocardial revascularization, suffering from:

  • Multivessel coronary artery disease amenable for surgical treatment
  • Negative history of previous cardiac or vascular surgery in childhood and afterwards.
  • Negative history of active neoplastic disease, neither past medical history of oncological treatment
  • Patients with non insulin dependent diabetes mellitus treated chronically with oral derivatives of sulfonylourea such as but not limited to: glibenclamide.

Exclusion Criteria:

Patients suffering from acute insuficiency of any organ/ system and those suffering from end stage organ failure such as:

  • Chronic renal disease - KDOQI stage ≥ 3;
  • Chronic renal failure class A by Child - Pugh'a;
  • Chronic respiratory failure (type I and II according to Campbell et al. and type I according to Wood et al.);
  • Chronic intermittent claudication class 2A according to Fontaine;

Sites / Locations

  • Medinet Heart CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

RIC Group

Control Group

Arm Description

Three cycles of remote ischemic conditioning (5minutes ischemia and 5minutes reperfusion; lower leg ischemia achieved by pressure cuff inflation and deflation); First three cycles the patient will receive 24 hours preoperatively, second three cycles the patient will receive after the induction of general anesthesia but before skin incision shortly before CABG. Remote ischemic postconditioning (5minutes ischemia and 5minutes reperfusion; lower leg ischemia achieved by pressure cuff inflation and deflation) will be administered to the patient within 60 minutes after the completion of all coronary artery bypass grafts and the restoration of coronary blood flow.

Control group will receive sham procedure near identical to intervention. That will be afforded by inflation of pressure cuff on artificial leg hidden under the draping by an assistant who is not included in the research team and does not have any connection to study design and data analysis.

Outcomes

Primary Outcome Measures

Postoperative myocardial necrosis
Serial mesurements of High - Sensitive Troponin T release
Postoperative kidney injury
Serial measurements of estimated glomerular filtration rate by creatinine

Secondary Outcome Measures

Perioperative mortality
30-day all cause mortality
Perioperative myocardial infarction
30-day myocardial infarction
Postoperative Acute Kidney Injury
Prevalence of acute kidney injury according to Society of Thoracic Surgeons definitions of outcomes.

Full Information

First Posted
November 30, 2017
Last Updated
November 30, 2017
Sponsor
Medinet Heart Centre
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1. Study Identification

Unique Protocol Identification Number
NCT03363958
Brief Title
Remote Ischemic Conditioning to Attenuate Myocardial Death and Improve Operative Outcome.
Acronym
RICARDO
Official Title
Effect of Remote Ischemic Conditioning on Ischemia and Reperfusion Injury in Patients Submitted to Coronary Artery Bypass Grafting.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2014 (Actual)
Primary Completion Date
January 1, 2019 (Anticipated)
Study Completion Date
January 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medinet Heart Centre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates the addition of remote ischemic preconditioning and postconditioning to standard myocardial protection protocol in patients submitted to off - pump coronary artery bypass grafting in a prospective, 1:1 randomized, double blind fashion. An interventional group will receive remote ischemic preconditioning 24-hours before OP-CABG, immediately before surgery and within 60 minutes following surgery by means of lower limb ischemia achieved by pressure cuff inflation, whereas control group will receive sham procedure perioperatively.
Detailed Description
In a prospective, 1:1 randomized and double blind fashion, the study will evaluate the impact of remote ischemic preconditioning, both immediate and second window of protection (24 hours and immediately before surgery) with remote ischemic postconditiong on operative outcomes in patients submitted to coronary artery bypass grafting without use of extracorporeal circulation. Remote ischemic conditioning was found to provide protection against necrosis and apoptosis due to ischemia and reperfusion injury, a phenomenon observed during coronary artery bypass grafting. That in turn was associated with poor postoperative outcomes, predominantly poor survival. Remote ischemic preconditioning will be provided by repeated lower leg ischemia and reperfusion with pressure cuff inflation for five minutes and deflation for five minutes in three consecutive cycles. Remote ischemic preconditioning will be performed 24 hours before CABG and immediately before surgery. Remote ischemic postconditioning will be performed within 60 minutes following the last coronary artery bypass graft completion and the restoration of coronary blood flow. The study will assess clinical endpoints such as postoperative acute myocardial infarction (type 5 MI), postoperative mortality, postoperative renal failure and laboratory outcomes such as postoperative serial measurements of troponin T release or glomerular filtration rate as secondary outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Bypass, Myocardial Reperfusion Injur, Ischemic Preconditioning, Myocardial, Ischemic Postconditioning
Keywords
myocardial protection, remote ischemic preconditioning, remote ischemic postconditioning, cardiac surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RIC Group
Arm Type
Experimental
Arm Description
Three cycles of remote ischemic conditioning (5minutes ischemia and 5minutes reperfusion; lower leg ischemia achieved by pressure cuff inflation and deflation); First three cycles the patient will receive 24 hours preoperatively, second three cycles the patient will receive after the induction of general anesthesia but before skin incision shortly before CABG. Remote ischemic postconditioning (5minutes ischemia and 5minutes reperfusion; lower leg ischemia achieved by pressure cuff inflation and deflation) will be administered to the patient within 60 minutes after the completion of all coronary artery bypass grafts and the restoration of coronary blood flow.
Arm Title
Control Group
Arm Type
Sham Comparator
Arm Description
Control group will receive sham procedure near identical to intervention. That will be afforded by inflation of pressure cuff on artificial leg hidden under the draping by an assistant who is not included in the research team and does not have any connection to study design and data analysis.
Intervention Type
Procedure
Intervention Name(s)
Remote Ischemic Preconditioning with Postconditioning
Intervention Description
Three cycles of 5 minutes of ischemia and 5 minutes of reperfusion of lower leg 24 hours, immediately before surgery and within 60 minutes after the restoration of coronary blood flow postoperatively.
Intervention Type
Procedure
Intervention Name(s)
Sham RIPC procedure
Intervention Description
Three cycles of 5 minutes of inflation and 5 minutes of deflation of artificial lower leg immediately before surgery and within 60 minutes after the restoration of coronary blood flow postoperatively.
Primary Outcome Measure Information:
Title
Postoperative myocardial necrosis
Description
Serial mesurements of High - Sensitive Troponin T release
Time Frame
72 hours postoperatively
Title
Postoperative kidney injury
Description
Serial measurements of estimated glomerular filtration rate by creatinine
Time Frame
7 days postoperatively
Secondary Outcome Measure Information:
Title
Perioperative mortality
Description
30-day all cause mortality
Time Frame
30 days postoperatively
Title
Perioperative myocardial infarction
Description
30-day myocardial infarction
Time Frame
30 days postoperatively
Title
Postoperative Acute Kidney Injury
Description
Prevalence of acute kidney injury according to Society of Thoracic Surgeons definitions of outcomes.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients qualified to coronary artery bypass grafting according to ESC/EACTS Guidelines of myocardial revascularization, suffering from: Multivessel coronary artery disease amenable for surgical treatment Negative history of previous cardiac or vascular surgery in childhood and afterwards. Negative history of active neoplastic disease, neither past medical history of oncological treatment Patients with non insulin dependent diabetes mellitus treated chronically with oral derivatives of sulfonylourea such as but not limited to: glibenclamide. Exclusion Criteria: Patients suffering from acute insuficiency of any organ/ system and those suffering from end stage organ failure such as: Chronic renal disease - KDOQI stage ≥ 3; Chronic renal failure class A by Child - Pugh'a; Chronic respiratory failure (type I and II according to Campbell et al. and type I according to Wood et al.); Chronic intermittent claudication class 2A according to Fontaine;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jakub S. Marczak, M.D.
Phone
0048883774566
Email
marczak@space.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Sleiman S. Aboul - Hassan, M.D.
Phone
0048683882194
Email
s.aboulhassan@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jakub S. Marczak, M.D.
Organizational Affiliation
Medinet Heart Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medinet Heart Centre
City
Nowa Sol
State/Province
Lubuskie
ZIP/Postal Code
67-100
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sleiman Sebastian Aboul-Hassan, MD
Email
s.aboulhassan@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22286602
Citation
Marczak J, Nowicki R, Kulbacka J, Saczko J. Is remote ischaemic preconditioning of benefit to patients undergoing cardiac surgery? Interact Cardiovasc Thorac Surg. 2012 May;14(5):634-9. doi: 10.1093/icvts/ivr123. Epub 2012 Jan 26.
Results Reference
background
Links:
URL
http://medinet.pl
Description
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Remote Ischemic Conditioning to Attenuate Myocardial Death and Improve Operative Outcome.

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