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Personalised Simulation Technologies for Optimising Treatment in the Intensive Care Unit

Personalised Simulation Technologies for Optimising Treatment in the Intensive Care Unit

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04297397
Acronym
PSTOTICU
Enrollment
25
Registered
2020-03-05
Start date
2020-02-20
Completion date
2022-05-31
Last updated
2023-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Distress Syndrome, Adult, Respiratory Insufficiency

Keywords

ICU, Patient Simulation, Critical Care, ARDS, Mechanical Ventilation

Brief summary

This project aims to develop software models describing how critically ill patients respond to changes in their treatment whilst admitted to an Intensive Care Unit (ICU). We will use high performance computers to fit software models to the physiological and treatment data of patients receiving mechanical ventilation.

Detailed description

In the United Kingdom, approximately 142,000 people are admitted to ICU each year. A large proportion, 10 - 20%, of these patients have a life-threatening respiratory illness called Acute Respiratory Distress Syndrome (ARDS). These patients need specialist help with their breathing, from a machine called a ventilator. Only seven out of ten patients will survive this illness and even survival may bring ongoing problems, sometimes for a long time after leaving hospital. Accurate mathematical and computer models of ARDS, would allow investigation of the illness outside of the ICU and inside the virtual environment of a computer. Different treatments could be simulated on the same 'virtual' patient, or the same treatment on many different patients with varying degrees of illness. Development of these software models, requires collection of a library of data describing how patients respond to changes in their treatment. An example would be to describe how a patient's blood pressure responds to a change in the settings of their ventilator. The changes to a patient's ventilation would be made as part of the normal care provided by the doctors and nurses looking after them. Mathematical descriptions have been created before, from simpler data sets which were essentially single snapshots of a patient's condition and treatment. The investigators aim to capture sequences of snapshots over several hours, allowing them to build more accurate models. Guy's and St Thomas' NHS Foundation Trust (GSTFT) is the clinical partner of the project. Patients would be identified there by clinical researchers, who would then collect the data describing their treatment. This data would be anonymised before adding to the library of data to be shared with academic researchers. Academic members of the team at the University of Warwick and the University of Nottingham possess the engineering and mathematical expertise needed to develop the complex software models. They also provide the facility of a high performance computing cluster necessary for the difficult process of fitting models to the data. Once the software models have been built and used to examine the how treatment might be improved, the findings would be shared with clinical staff around the world, through the publication of articles in medical journals. It is possible that the insights gained by the modelling process might inform, change and improve how clinical staff use ventilators to support patients with ARDS.

Interventions

None listed

Sponsors

University of Nottingham
CollaboratorOTHER
University of Warwick
CollaboratorOTHER
Guy's and St Thomas' NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* At least 18 years of age * Patients admitted to GSTFT Intensive Care between the dates 01/01/2010 and 31/03/2019 * Receiving mechanical ventilation

Exclusion criteria

* Pregnancy or lactation

Design outcomes

Primary

MeasureTime frameDescription
Development of a simulation platform2 yearsDevelop predictive physiological models and simulation platform in mechanically ventilated patients with ARDS

Secondary

MeasureTime frameDescription
Development of dynamic modelling with integration of real time ICU data streams2 yearsTo integrate data-streams available in the ICU with our existing physiological modelling algorithms to enable real-time simulation of treatment response.
Exploration of therapeutic intervention design space2 yearsTo develop mathematical methods to explore the design space for a clinical support system.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026