Dexcom G7 CGM in critically ill adults after major abdominal surgery or solid organ transplant

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this interventional study, critically ill adults in the ICU wearing two Dexcom G7 sensors will help determine how well the device measures glucose during insulin therapy after major abdominal surgery or organ transplantation. One sensor is blinded to avoid monitoring, while the other provides real-time data to guide insulin dosing. Patients will wear sensors for up to 10 days, with four glucose checks per day and daily SOFA scoring to correlate sensor readings with patient status. Calibration occurs only on the unblinded sensor using standard blood glucose meter readings. The study design includes ongoing integration with routine ICU care without altering standard workflows.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age 18 years or over
* Intensive care unit admission
* Requiring blood glucose monitoring for insulin therapy

Exclusion Criteria:

* High-dose ascorbic acid or acetaminophen \> 4g/day
* Physical or mental health condition precluding continuous wear of the continuous glucose monitor, as judged by the physician

Where it's running

• Institute of Clinical and Experimental Medice
  Prague, Czechia Recruiting

Study contacts

• Study coordinator: Marek Protus, MD
• Email: marek.protus@ikem.cz
• Phone: +420602278062

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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.