Skip to main content
OpenTrials
Completed

NCT Number: NCT02004483

Analysis of Myocardial Layer Specific Systolic and Diastolic Function During and After PCI

Investigators will analyzed systolic and diastolic function during and after ischemia induced by percutaneous coronary intervention.Also will be analyzed a local work index during acute ischemia induced by percutaneous coronary intervention.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Aachen

Aachen, North Rhine-Westphalia, 52074, Germany

About this study

PART 1: ANALYSIS OF LAYER SPECIFIC SYSTOLIC AND DIASTOLIC FUNCTION DURING ACUTE ISCHEMIA INDUCED BY PERCUTANEOUS CORONARY INTERVENTION 35 patients with normal systolic left ventricular function at baseline with indication for elective percutaneous coronary angioplasty will be included in the study. In these patients acute ischemia will be induced by elective percutaneous coronary angioplasty with balloon inflation and thus vessel occlusion for 60 sec. During these 60 seconds ischemia will develop throughout all layers of the myocardium affecting diastolic systolic and diastolic function. During the subsequent reperfusion period signs of ischemia with systolic and diastolic dysfunction of all layers will subside. Echocardiographic imaging at short intervals of 10 sec during ischemia and at intervals of 20 sec during reperfusion up to 10 min after reopening of the vessel as well as 1 hour and 24 hours later will allow serial comparison of strain curves and thereby allow definition of the time sequence systolic and diastolic function abnormalities occur in three myocardial layers as well as the resolution of abnormalities during reperfusion. The analysis of circumferential as well as radial strain will allow definition of differences between radial and circumferential strain during ischemia induction and resolution.

PART 2: ANALYSIS OF LOCAL WORK INDEX DURING ACUTE ISCHEMIA INDUCED BY PERCUTANEOUS CORONARY INTERVENTION.

In the same 35 patients as in Clinical step 1 the local work index of the ischemic area as well as the contralateral non-ischemic areas will be determined in serial studies to determine the onset of abnormality, the amount of abnormality and the resolution of abnormality. Changes in local work index in the ischemic area will be related to changes in peak systolic strain and strain imaging diastolic index.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed informed consent.
  • Adequate quality of echocardiographic images.
  • Significant stenosis of the proximal left anterior descending artery, the right coronary artery or the left circumflex artery
  • Anginal pain or proven myocardial ischemia due to the coronary stenosis
  • Elective percutaneous coronary intervention planned
  • Planned direct stenting of the coronary artery

Exclusion criteria

  • Prior myocardial infarction
  • Significant coronary collaterals
  • Significant valvular regurgitation (>Sellers II)
  • Congestive heart failure
  • Pacemaker dependency
  • Bundle branch block or significant arrhythmia
  • Atrial fibrillation
  • Previous coronary bypass grafting
  • Impaired kidney function corresponding to a GFR(Glomerular filtration rate) below 60 mL/min.
  • Women, who are pregnant or breastfeeding.
  • Patient taking part in another clinical study
  • Subjects who are committed to an institution and/or penitentiary by judicial or official order.
  • Complex coronary lesion requiring balloon angioplasty or rotational atherectomy prior to stenting

Treatment and study plan

Percutaneous coronary intervention

Procedure

Percutaneous coronary intervention is performed according to standard practice. Direct stenting is required for the procedure as it is done in most coronary interventions today. After insertion of the non-inflated stent into the coronary lesion there should still be flow to the distal vessel. The stent should be implanted at high-pressure with balloon inflation lasting for 60 seconds to allow adequate expansion of the stent. Post-dilatation should be performed if required. However, this should be done more than 5 minutes after stent implantation.

Primary outcomes

  1. systolic and diastolic function

    Time frame: during 60 seconds ischemia caused by PCI

    Echocardiographic imaging at short intervals of 10 sec during ischemia, which will be induced by elective percutaneous coronary angioplasty with balloon inflation and thus vessel occlusion for 60 sec.

Secondary outcomes

  1. systolic and diastolic function

    Time frame: during 10 minutes, after 1 hour and after 24 hours after PCI

    Echocardiographic imaging of layer specific systolic and diastolic function at intervals of 20 sec during reperfusion up to 10 min after reopening of the vessel as well 1 hour and 24 hours after percutaneous coronary intervention.

Sponsors and collaborators

Lead sponsor

RWTH Aachen University

Other

Collaborators

  • Department of Biomedical Engineering, Technion, Haifa, Israel

Registry information

Official study title

Comprehensive Analysis of Myocardial Layer Specific Systolic and Diastolic Function in Patients With Coronary Artery Disease Undergoing Percutaneous Coronary Intervention

Acronym: PCI-Strain

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Dec 9, 2013
Registry last updated
Sep 23, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.