An interventional study of Transcranial doppler (TCD) in STEMI, Left Ventricular Thrombus and Acute Ischemic Stroke, sponsored by CHC Montlegia. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-12.
Sponsored by CHC Montlegia · Not applicable, Interventional, and Diagnostic
The goal of this study is to define a correlation between the number of microembolic signals (MES) detected and the risk of occurrence of an Acute Ischemic Stroke (AIS) at 2 years or a Left Ventricular Thrombus (LVT) at 6 weeks Participants will perform a transcranial doppler with MES detection.
850 studies on the registry are indexed under ST Elevation Myocardial Infarction; 197 are open to participants now.
This study's planned enrollment of 116 is below the median of 194 across 527 interventional studies indexed under ST Elevation Myocardial Infarction.
Browse ST Elevation Myocardial Infarction studies →CHC Montlegia is the lead sponsor of 2 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Secondary exclusion criteria
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
LVEF (left ventricular ejection fraction)
The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Life expectancy
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Device: Transcranial doppler (TCD)
A TCD with MES detection will be performed the day of the inclusion. Another TCD will be performed at 6 weeks of the inclusion. They will then receive telephone follow-up at one year, followed by a final visit two years after inclusion, blinded to the results of the TCD.
Demonstration of a correlation between the number of MES detected and the 2-year risk of AIS or the occurrence of a LVT at 6 weeks in patients with post-STEMI LVD.
Time frame: To the enrollment period to 2-years of AIS or 6-weeks of a LVT
Demonstration of a correlation between the number of MES detected and the treatment given (single anti-aggregation, double anti-aggregation, anti-coagulation) in patients suffering from LVD
Time frame: To the enrollment period to 2-years of AIS or 6-weeks of a LVT
Demonstration of a correlation between the variation in the number of MES detected and the modification of the treatment administered (single anti-aggregation, double anti-aggregation, anti-coagulation) in patients suffering from LVD
Time frame: To the enrollment period to 2-years of AIS or 6-weeks of a LVT
Demonstration of a correlation between the number of MES and the LVD rate according to the ACCF/AHA Heart Failure classification
Time frame: At screening
Demonstration of a correlation between the number of MES detected and the risk of occurrence of an AIS at 2 years or LVT at 6 weeks in patients suffering from LVD, classified by subgroup of cardiac decompensation according to the ACCF/AHA Heart Failur
Time frame: To the enrollment period to 2-years of AIS or 6-weeks of a LVT
Creation of a large multicentric prospective follow-up database of patients suffering from LVD, whether symptomatic or not
Time frame: To the enrollment period to the end of the follow-up, three years after
No study locations are listed for this record.
PDFs hosted by the registry, ClinicalTrials.gov.
Plan to share: No
Start is estimated for Dec 2026; primary completion for Dec 2027, 12 months later.
Of 134 non-industry interventional studies with no phase under ST Elevation Myocardial Infarction, half reached primary completion within 38 months of starting (the median), counting those still running; a quarter within 19 and three quarters within 64. This study's planned 12 months is below that.
Counting every sponsor, half of 143 studies reached it within 38 months; a quarter within 19 and three quarters within 64.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.
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