Creating a database of physiological data for critically ill adults

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 aims to establish a warehouse of physiological data and biomedical signals from adult patients in intensive care, specifically utilizing records from the Philips Intellivue MP70 monitor. It focuses on the early detection and prediction of organ failure in critically ill patients, which could lead to improved patient outcomes and reduced healthcare costs. The methodology involves data mining and the development of algorithms to analyze complex physiological data, enabling better decision-making in acute medical situations. The ultimate goal is to enhance the understanding of critical illness and facilitate the transfer of knowledge to the medical device industry.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Any adult patient admitted in Brest University Hospital's intensive care unit for monitoring of vital failure

Exclusion Criteria:

* Refusal to participate

Where it's running

• CHRU de Brest
  Brest, France Recruiting

Study contacts

• Principal investigator: Erwan L'Her, Professor — CHRU de Brest
• Study coordinator: Erwan L'Her, Professor
• Email: erwan.lher@chu-brest.fr
• Phone: 02 98 34 71 81

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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.