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Temporary Epicardial Cardiac Resynchronisation.

Primary Purpose

Cardiac Failure

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Biventricular pacing
Sponsored by
Cardiff and Vale University Health Board
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Failure focused on measuring cardiac failure, thoracic surgery, cardiac pacing, artificial

Eligibility Criteria

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

Inclusion Criteria:

  • Coronary disease scheduled for surgical revascularisation. Ejection fraction <35% (simpson's method.)

Exclusion Criteria:

  • Permanent pacemaker or implantable defibrillator. Dialysis dependent renal failure. Permanent atrial fibrillation.

Sites / Locations

  • Cardiff and Vale University Health Board.
  • Morriston Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Standard pacing

BiVentricular pacing (BiV).

Arm Description

Standard pacing settings prescribed by the cardiac surgeon or intensivist after revascularisation.

The group of patients receiving biventricular pacing after cardiac surgery.

Outcomes

Primary Outcome Measures

Duration of Level 3 care after cardiac surgery, as defined by the 'Designed for Life' document- Welsh Assembly Government.

Secondary Outcome Measures

Mortality
Haemodynamic support after surgery (inotropes/ intra-aortic balloon pump.)
Vascular event (stroke or myocardial infarction.)
post operative arrhythmia.
Haemodynamic measurements of cardiac status (Pulmonary arterial catheter, echo data and FloTrac monitor).
Renal function and requirement for haemofiltration.
Biomarkers (Troponin T and NT Pro BNP.)
Re-intubation or re-sternotomy.

Full Information

First Posted
December 4, 2009
Last Updated
January 28, 2020
Sponsor
Cardiff and Vale University Health Board
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1. Study Identification

Unique Protocol Identification Number
NCT01027299
Brief Title
Temporary Epicardial Cardiac Resynchronisation.
Official Title
A Randomised Study of Temporary Epicardial Cardiac Resynchronisation Versus Conventional Right Ventricular Pacing in Cardiac Surgical Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cardiff and Vale University Health Board

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This trial will investigate the clinical and haemodynamic effects of temporary biventricular pacing after cardiac surgery. Subjects with poor left ventricular systolic function will receive either temporary biventricular pacing or 'standard' post-operative pacing for 48 hours. The investigators hypothesis that reversal of cardiac dyssynchrony will improve tissue perfusion and cardiac haemodynamics after surgical revascularisation. This will shorten post-operative recovery in cardiac ITU.
Detailed Description
Patients with poor left ventricular (LV) function are at higher risk of complications after cardiac surgery, compared to patients with preserved LV function. The higher complication rates also lead to prolonged Cardiac Intensive Care (CITU) admissions for monitoring and multi-organ support. The investigators hypothesise that BiV pacing will reverse cardiac dyssynchrony and improve target organ perfusion. This will be significantly reduced the post operative requirement for Level 3 CITU care. This study will compare 48 hours of temporary biventricular (BiV) pacing to enhance cardiac function against standard post-operative pacing, in patients with poor LV function undergoing cardiac surgery. Temporary biventricular (BiV) pacing will be achieved with the addition of a third pacing electrode attached to the left ventricle. Using a pulmonary arterial catheter the interventricular (VV) delay will be adjusted to yield the maximum cardiac output at constant heart rate- sequential BiV pacing. A pilot study conducted at the University Hospital of Wales (UHW) showed that this approach is likely to be successful. The primary endpoint of the study will be the mean duration of Level 3 CITU care required by patients after cardiac surgery. Secondary endpoints will include: haemodynamic improvement with BiV pacing; post-operative renal function; atrial fibrillation (AF)/ ventricular arrhythmias; post operative inotropic requirements and changes in biomarkers- NT Pro BNP and Troponin T.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Failure
Keywords
cardiac failure, thoracic surgery, cardiac pacing, artificial

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Standard pacing
Arm Type
Active Comparator
Arm Description
Standard pacing settings prescribed by the cardiac surgeon or intensivist after revascularisation.
Arm Title
BiVentricular pacing (BiV).
Arm Type
Active Comparator
Arm Description
The group of patients receiving biventricular pacing after cardiac surgery.
Intervention Type
Device
Intervention Name(s)
Biventricular pacing
Other Intervention Name(s)
Standard pacing
Intervention Description
Optimised temporary biventricular pacing.
Primary Outcome Measure Information:
Title
Duration of Level 3 care after cardiac surgery, as defined by the 'Designed for Life' document- Welsh Assembly Government.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Mortality
Time Frame
30 days
Title
Haemodynamic support after surgery (inotropes/ intra-aortic balloon pump.)
Time Frame
30 days
Title
Vascular event (stroke or myocardial infarction.)
Time Frame
30 days
Title
post operative arrhythmia.
Time Frame
48 hours
Title
Haemodynamic measurements of cardiac status (Pulmonary arterial catheter, echo data and FloTrac monitor).
Time Frame
48 hours
Title
Renal function and requirement for haemofiltration.
Time Frame
30 days
Title
Biomarkers (Troponin T and NT Pro BNP.)
Time Frame
72 hours
Title
Re-intubation or re-sternotomy.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Coronary disease scheduled for surgical revascularisation. Ejection fraction <35% (simpson's method.) Exclusion Criteria: Permanent pacemaker or implantable defibrillator. Dialysis dependent renal failure. Permanent atrial fibrillation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zaheer R Yousef, MD
Organizational Affiliation
Cardiff and Vale Local Heath Board, Cardiff.
Official's Role
Study Director
Facility Information:
Facility Name
Cardiff and Vale University Health Board.
City
Cardiff
ZIP/Postal Code
CF14 4XW
Country
United Kingdom
Facility Name
Morriston Hospital
City
Swansea
ZIP/Postal Code
SA6 6NL
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
23138590
Citation
Russell SJ, Tan C, O'Keefe P, Ashraf S, Zaidi A, Fraser AG, Yousef ZR. Optimized temporary bi-ventricular pacing improves haemodynamic function after on-pump cardiac surgery in patients with severe left ventricular systolic dysfunction: a two-centre randomized control trial. Eur J Cardiothorac Surg. 2012 Dec;42(6):e146-51. doi: 10.1093/ejcts/ezs492.
Results Reference
derived
PubMed Identifier
22348447
Citation
Russell SJ, Tan C, O'Keefe P, Ashraf S, Zaidi A, Fraser AG, Yousef ZR. Temporary epicardial cardiac resynchronisation versus conventional right ventricular pacing after cardiac surgery: study protocol for a randomised control trial. Trials. 2012 Feb 20;13:20. doi: 10.1186/1745-6215-13-20.
Results Reference
derived

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Temporary Epicardial Cardiac Resynchronisation.

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