RIPC: The Effect of Remote Ischemic Preconditioning in the Cardiac Surgery

Sponsor
Seoul National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00997217
Collaborator
Asan Medical Center (Other)
1,200
1
13
92.2

Study Details

Study Description

Brief Summary

Perioperative myocardial injury is a serious complication of cardiac surgery. This complication increases both mortality and morbidity of cardiac surgery. Remote ischemic preconditioning (RIPC) is the concept that brief ischemia followed by reperfusion in an organ can reduce subsequent ischemia-reperfusion injury in distant organs. Recent several clinical trials showed powerful myocardial protective effect of remote ischemic preconditioning by reducing postoperative cardiac enzymes. However, the evidence that remote ischemic preconditioning can improve the clinical outcomes such as mortality and morbidity, is still lacking. The investigators perform a multicenter randomized controlled study to evaluate that remote ischemic preconditioning can improve the outcomes of cardiac surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: remote ischemic preconditioning
Phase 1

Detailed Description

Perioperative myocardial injury is a serious complication of cardiac surgery. This complication increases both mortality and morbidity of cardiac surgery. Remote ischemic preconditioning (RIPC) is the concept that brief ischemia followed by reperfusion in an organ can reduce subsequent ischemia-reperfusion injury in distant organs. Recent several clinical trials showed powerful myocardial protective effect of remote ischemic preconditioning by reducing postoperative cardiac enzymes. However, the evidence that remote ischemic preconditioning can improve the clinical outcomes such as mortality and morbidity, is still lacking. The investigators perform a multicenter randomized controlled study to evaluate that remote ischemic preconditioning can improve the outcomes of cardiac surgery.

Purpose:

The purpose of this study is to examine if remote ischemic preconditioning can decrease the mortality and fatal postoperative complications in patients undergoing cardiac surgery. The effect will be assessed by mortality, severe morbidities and duration of hospital stay.

Methods:

Study patients will be randomized to cardiac surgery with RIPC or conventional cardiac surgery in two cardiac surgical centers (Seoul National University Hospital and Asan Medical Center). Remote ischemic preconditioning consists of four 5 min cycles of upper limb ischemia and reperfusion with pneumatic cuff up to 200 mmHg. RIPC is performed twice: before and after the coronary anastomosis in off-pump coronary bypass graft surgery; or before and after the cardiopulmonary bypass in the cardiac valve surgery.

Primary study outcome is in-hospital death within 30 postoperative days and fatal postoperative complications such as myocardial infarction, stoke, respiratory failure, renal failure, cardiogenic shock and gastrointestinal complications. Secondary outcomes include the length of intensive care unit (ICU) stay and hospital stay.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
The Effect of Remote Ischemic Preconditioning on Mortality and Morbidity in Cardiac Surgery: a Randomized Controlled Trial
Study Start Date :
Oct 1, 2009
Actual Primary Completion Date :
Sep 1, 2010
Actual Study Completion Date :
Nov 1, 2010

Outcome Measures

Primary Outcome Measures

  1. In-hospital death [Postoperative 30 days]

  2. Myocardial infarction [Postoperative 30 days]

  3. Stroke [Postoperative 30 days]

  4. Respiratory failure [Postoperative 30 days]

  5. Renal dysfunction [Postoperative 30 days]

  6. Renal failure [Postoperative 30 days]

  7. Cardiogenic shock [Postoperative 30 days]

  8. Gastrointestinal complication [Postoperative 30 days]

Secondary Outcome Measures

  1. Length of ICU stay [Postoperative 3 months]

  2. Length of postoperative hospital stay [Postoperative 3 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • adult patients undergoing cardiac surgery
Exclusion Criteria:
  • emergent operation

  • preoperative use of inotropics or mechanical assist device,

  • left ventricular ejection fraction less than 30%,

  • severe liver, renal and pulmonary disease,

  • recent myocardial infarction (within 7 days),

  • recent systemic infection or sepsis (within 7 days)

  • peripheral vascular disease affecting upper limbs

  • amputation of the upper limbs

  • major combined operation such as aortic surgery or carotid endarterectomy

  • descending thoracic aortic surgery

  • rare surgeries; cardiac transplantation, correction of complicated congenital anomalies, pulmonary thromboembolectomy, etc

Contacts and Locations

Locations

Site City State Country Postal Code
1 Seoul National University Hospital Seoul Korea, Republic of 110-744

Sponsors and Collaborators

  • Seoul National University Hospital
  • Asan Medical Center

Investigators

  • Study Director: YunSeok Jeon, professor, Department of Anesthesiology and Pain Medicine, SNUH

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00997217
Other Study ID Numbers:
  • RIPCmulticenter
First Posted:
Oct 19, 2009
Last Update Posted:
Feb 24, 2011
Last Verified:
Feb 1, 2011
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 24, 2011