Clinical trial Recruiting at 9 sites Interventional Ages 18 to 85

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.

More Acute Coronary Syndrome trials

Quick facts

Study typeInterventional
Ages18 Years to 85 Years
SexAll
Enrollment850 (estimated)
SponsorUniversity Hospital, Montpellier
Academic / other
Locations9 sites (Béziers and 8 other locations)
StatusRecruiting
StartedNovember 6, 2023
Main results expectedMay 6, 2028
Study endsMay 6, 2028
Registry record updatedJune 12, 2026
Trial IDNCT06014112 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

  • 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
  • Hospital of Pau
    Pau, France
    Recruiting
  • University Hospital of Toulouse
    Toulouse, France
    Recruiting
  • Vannes Bretagne Atlantique Hospital
    Vannes, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.