RheoMECC: Rheoparin-coated Tubing System for Minimized Extracorporeal Circulation (MECC)

Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Completed
CT.gov ID
NCT02321917
Collaborator
(none)
50
2
2
80
25
0.3

Study Details

Study Description

Brief Summary

In this study, the investigators would like to compare a heparin-coated tubing system for minimized extracorporeal circulation (MECC) with the conventional tubing system for MECC, which does not contain heparin coating. The MECC system has been used since 14 years in the investigators' hospital as an extracorporeal system to support circulation and provide oxygen to the tissues during coronary artery bypass grafting. Until today, the investigators performed more than 5000 MECC procedures in their department.

Condition or Disease Intervention/Treatment Phase
  • Device: MECC system with rheoparin coating
N/A

Detailed Description

Background

The investigators would like to investigate a new composition of their MECC system in patients receiving coronary artery bypass surgery. Normally, the MECC system induces complement system activation and coagulation cascade, which could have a negative impact on postoperative outcome. A tubing system containing heparin (rheoparin) could contribute to a better biocompatibility in terms of a diminished activation of inflammatory reactions and a reduction of cerebral embolic load, which is a regular issue during extracorporeal circulation due to formation of solid and gaseous microemboli in the tubing system.

Objective

The aim is to investigate biocompatibility (coagulation, inflammation) and influence on cerebral embolic load of the rheoparin-coated MECC system and to compare the results with the current MECC system containing a rheoparin-free tubing system.

Methods

Patients undergoing elective coronary artery surgery are randomized to receive extracorporeal circulation using the MECC system with or without rheoparin coating. All procedures are performed according to the institutional standards.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Coagulation, Inflammation and Cerebral Embolism Using a Rheoparin-coated Tubing System for Minimized Extracorporeal Circulation (MECC): Differences to the Conventional MECC System
Actual Study Start Date :
Apr 1, 2013
Actual Primary Completion Date :
Nov 1, 2019
Actual Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Rheoparin coating

MECC system with rheoparin coating

Device: MECC system with rheoparin coating
MECC system for extracorporeal circulation equipped with rheoparin coating.

No Intervention: No rheoparin coating

MECC system without rheoparin coating

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in coagulation / inflammation parameters at the post-operative phase [Perioperative period, 7 days]

    Biocompatibility will be assessed by measuring different coagulatory and inflammatory parameters as determined in comparable studies. Especially, hte investigators assess in their central laboratory the thrombin-antithrombin complex and the d-dimer as measures of the activity of the coagulation/fibrinolysis system and furthermore the complement factors C3a-C5a, the interleukins IL 6, IL8, IL10, the tumor-necrosis factor alpha (TNF-alpha), platelet factor 4 and the syndecan-1 activity as an expression of the inflammatory response to the different coating used for minimized extracorporeal circulation system.

Secondary Outcome Measures

  1. Cerebral embolism [Perioperative period, 7 days]

  2. Mortality [At 30 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Written informed consent

  • Elective cardiac surgery

  • Coronary artery bypass grafting

Exclusion Criteria

  • Re do

  • Usage of antiplatelets, antithrombotic drugs

  • Coagulopathy

  • Persistent foramen ovale

  • Infection

  • Heparin-induced thrombocytopenia (HIT)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dep. Cardiovascular Surgery Bern Switzerland 3010
2 Inselspital, University Hospital Bern, University of Bern Bern Switzerland 3010

Sponsors and Collaborators

  • University Hospital Inselspital, Berne

Investigators

  • Principal Investigator: Thierry Carrel, MD, PhD, Dep. Cardiovascular Surgery

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier:
NCT02321917
Other Study ID Numbers:
  • 143/13
First Posted:
Dec 22, 2014
Last Update Posted:
Dec 19, 2019
Last Verified:
Dec 1, 2019
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 19, 2019