Using a glucose measurement system in intensive care for patients with shock

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

This study evaluates the feasibility of the 'CGM GUARDIAN 2' system for monitoring glucose levels in patients experiencing hyperglycemia due to septic shock in intensive care units. The traditional method of blood glucose monitoring involves painful capillary sampling every two hours, which can lead to discomfort and sleep disturbances. The 'CGM GUARDIAN 2' system uses a subcutaneously placed electrode to measure glucose levels in interstitial fluid, potentially reducing the need for frequent blood draws. This approach aims to improve patient comfort and glycemic control in critically ill patients.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patient in septic shock
* Arterial hypotension requiring noradrenaline
* Hyperglycaemia requiring insulin therapy

Exclusion Criteria:

* Patients under guardianship, curatorship or deprived of liberty
* Pregnant or breastfeeding women

Where it's running

• CHU de Nice
  Nice, France Recruiting

Study contacts

• Principal investigator: Florent BILGER — Centre Hospitalier Universitaire de Nice
• Study coordinator: Florent BILGER
• Email: bilger.f@chu-nice.fr
• Phone: 492035510

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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.