Creating a database of physiological data for critically ill adults
Setting up a Warehouse of Physiological Data and Biomedical Signals in Adult Intensive Care
This study is trying to collect and analyze health data from critically ill adults to see if it can help doctors spot organ failure earlier and improve patient care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Brest Academic / other |
| Locations | 1 site (Brest) |
| Trial ID | NCT02893462 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients admitted to the intensive care unit for monitoring of vital failure.
Not a fit: Patients who refuse to participate in the study will not benefit from the findings or advancements derived from this research.
Why it matters
Potential benefit: If successful, this approach could significantly improve early detection of organ failure, leading to better patient management and outcomes in critical care settings.
How similar studies have performed: While the approach of data mining in critical care is gaining traction, this specific methodology and application may be novel and untested.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Brest
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.