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NCT Number: NCT02893462

Setting up a Warehouse of Physiological Data and Biomedical Signals in Adult Intensive Care

The aim of this study is the establishment of a warehouse physiological data and biomedical signal in intensive care adult patients in acute situations from particular records from the Philips Intellivue MP70 monitor.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Cardiopulmonary failures are major public health concerns, due to the aging population. Each of these situations is burdened with a poor prognosis in the medium term and a source of prolonged hospitalizations, generating significant health costs. Early detection and prediction of organ failure could reduce health costs and risks for the patient, offering a reaction early and appropriate medical technology. The proposed approach aims to optimize the knowledge of a complex physiological domain and multi-system, while promoting the automatic transfer of knowledge. The approach proposed data-mining and development of algorithms for detecting and / or predicting a strong potential for disruption because it proposes to apply innovative automated analysis procedures to a fragile patient population, and then a transfer to the medical device industry.

From communicating tools of recording of the signals, the investigator envisage in a global way:

  • the constitution of a warehouse of physiological data of grown-up patients in acute situation (intensive care unit);
  • the development by data mining of a system of detection of organs failures or adverse events basing itself on the application of innovative algorithms, allowing the decision-making operational, from the fusion of arisen ill-assorted events;
  • the use of intelligent tools of auto-learning and elaboration of complex multimodal models for purposes of prediction of events;

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Refusal to participate

Treatment and study plan

Primary outcomes

  1. Number of participants with physiological signal abnormality

    Time frame: from two to twenty-four hours

    Whereas this is a data mining process (non-deterministic approach), no description can be provided

Study contacts

Contact information is provided by the study sponsor or research team.

Erwan L'Her, Professor

CONTACT

[email protected]

02 98 34 71 81

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Acronym: REASTOC

Important dates

Study start
2015
Primary completion
2025
Study completion
2027
First posted
Sep 8, 2016
Registry last updated
Aug 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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