UnknownNot Applicable

STunning After Balloon Occlusion

Sweden50 participantsStarted 2021-09-06

Plain-language summary

The aim of this study is to examine in-depth cardiac function and morphology after short-term coronary occlusion by balloon inflation in patients with stable coronary artery disease (CAD) who undergo percutaneous coronary intervention (PCI).

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Age \>18 years.
✓. Stable CAD with indication for PCI of a lesion in either of the following coronary segments:
✓. 6 or 7 (proximal or mid left anterior descending coronary artery)
✓. 11 (Proximal left circumflex coronary artery)
✓. 1 or 2 (proximal right coronary artery)
✓. Normal cardiac function in the myocardial segments subtended by the target vessel, as assessed by echocardiography at the time of coronary angiography.
✓. Written informed consent obtained.

Exclusion criteria

✕. Pre-existing heart failure
✕. Known pre-existing irreversible regional or global wall motion abnormalities affecting the myocardial segments subtended by the target vessel.
✕. Severe valvulopathy
✕. Thrombolysis In Myocardial Infarction (TIMI) flow \<3 in the target vessel.

What they're measuring

Precent Akinesia

Timeframe: 30 minutes post balloon occlusion

Trial details

NCT IDNCT05023629

SponsorVastra Gotaland Region

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2023-07-15

Contact for this trial

Björn Redfors, AssocProf

+46 31 342 7543 Bjoern.Redfors@wlab.gu.se

View on ClinicalTrials.gov More Coronary Artery Disease trials