Using continuous glucose monitoring to predict outcomes in acute coronary syndrome
Official title: Predictive Value of Glycemic Parameters Measured With the Freestyle Libre Pro iQ During Acute Coronary Syndrome
Run by University Hospital, Montpellier · NCT06014112 · Data updated 2026-11-12
This study is testing if continuous glucose monitoring can help doctors predict outcomes for patients with acute coronary syndrome by looking at their blood sugar levels.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 85 Years |
| Sex | All |
| Enrollment | 850 (estimated) |
| Sponsor | University Hospital, Montpellier Academic / other |
| Locations | 9 sites (Béziers and 8 other locations) |
| Status | Recruiting |
| Started | November 6, 2023 |
| Main results expected | May 6, 2028 |
| Study ends | May 6, 2028 |
| Registry record updated | June 12, 2026 |
| Trial ID | NCT06014112 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with acute coronary syndrome who are being treated in a cardiac intensive care unit.
✕Probably not a fit
Patients in cardiogenic or septic shock or those with severely impaired health may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the predictive value of glycemic parameters measured with the Freestyle Libre Pro iQ device in patients hospitalized for acute coronary syndrome (ACS). It focuses on understanding how glycemic variability and hyperglycemia can influence short- and long-term cardiovascular events. The study aims to enroll patients diagnosed with ACS in a cardiac intensive care unit and will analyze their glucose levels to identify potential prognostic indicators. By utilizing continuous glucose monitoring, the research seeks to improve risk stratification and management of ACS patients.
Why it matters
Potential benefit: If successful, this study could enhance the ability to predict major cardiovascular events in ACS patients, leading to better management and outcomes.
How similar studies have gone: Previous studies have indicated that continuous glucose monitoring can provide valuable prognostic information in similar patient populations, suggesting a promising approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with ACS managed in a cardiac intensive care unit (ICU). The diagnosis of ACS will be made in the presence of chest pain with ST-segment elevation on the ECG for STEMI or ST-segment change and/or a positive troponin cycle (values in accordance with the center's protocol) for NSTEMI. Exclusion Criteria: * Subjects in cardiogenic or septic shock * Subjects with ACS initially managed in a non-investigating center * Failure to obtain free, informed, written consent signed by the participant and investigator upon admission to the ICU * Person participating in another research study with an ongoing exclusion period * Subjects participating in a study that may have an impact on post ACS prognosis * Person deprived of his or her rights, person under guardianship or curatorship * Person deprived of liberty (by judicial or administrative decision) * Persons whose physical and/or psychological health is severely impaired, which, in the opinion of the investigator, may affect the participant's compliance to the study * Pregnant or breastfeeding women * Person who is not affiliated to a social security system or who is a beneficiary of such a system.
Where it's running
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Hospital of Béziers
Béziers, France Recruiting -
University Hospital of Bordeaux
Bordeaux, France Recruiting -
University Hospital of Montpellier
Montpellier, France Recruiting -
University Hospital of Nîmes
Nîmes, France Recruiting -
AP-HP Lariboisière Hospital
Paris, France Recruiting -
APHP - Hôpital Européen Georges Pompidou
Paris, France Recruiting
Show 3 more locations
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Hospital of Pau
Pau, France Recruiting -
University Hospital of Toulouse
Toulouse, France Recruiting -
Vannes Bretagne Atlantique Hospital
Vannes, France Recruiting
Study contacts
- Study coordinator: Ariane SULTAN, Professor
- Email: a-sultan@chu-montpellier.fr
- Phone: 0467338431
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.