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Temporary Epicardial Cardiac Resynchronisation.

NCT01027299 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2020-01-29

No results posted yet for this study

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.

Conditions

  • Cardiac Failure

Interventions

DEVICE

Biventricular pacing

Optimised temporary biventricular pacing.

Sponsors & Collaborators

  • Cardiff and Vale University Health Board

    lead OTHER_GOV

Principal Investigators

  • Zaheer R Yousef, MD · Cardiff and Vale Local Heath Board, Cardiff.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2012-01-31
Completion
2012-01-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01027299 on ClinicalTrials.gov