- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06289075
PrognostICate- Study:Prognostication of ICU- and Ventilator- Days Over the Next Years Until 2040 (PrognostICate)
Prognostication of ICU- and Ventilator- Days Over the Next Years Until 2040 Using Statistical Projection Models and Retrospective Data From International Databases From 2005-2023 (PrognostICate- Study).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Adequate resource allocation in Intensive Care Medicine is especially challenging due to limited resources and increasing demands for ICU capacities due to an aging population and medical advances. Several studies in the past were trying to predict ICULOS using different models. The Objective and aim of our retrospective multicenter study are to forecast ICU length of stay (ICULOS) and length of mechanical ventilation (LOMV) in ICU patients of different groups (regarding gender, age group, medical vs surgical admission) worldwide for the next years up to the year of 2040 using statistical forecasting models.
To achieve this objective, historical ICU data spanning from 2005 to 2023 is collected from international ICU databases worldwide as well as population data from national and international databases and employ different statistical forecasting models (ARIMA-Model (Auto-Regressive Integrated Moving Average), logistic regression, Poisson Regression and ETS (Exponential smoothing)) to make these predictions. The Validity of the 4 different models is assessed with out-of-time-cross validity by splitting the data in 2 subsets for generation and testing of the model in a ratio of approximately 75:25 of the dataset. The most valid model of the 4 different models will be chosen. The statistical analysis follows he guidelines for Accurate and Transparent Health Estimates Reporting (GATHER Statement) von Stevens et al. from the year 2016.
The ultimate goal of this project is to provide valuable insights to healthcare system decision-makers worldwide regarding future requirements of ICU beds and ventilator capacities. With this insight we want to enable healthcare- system decision makers worldwide to proactively anticipate and allocate appropriate ICU resources for the future.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Sandra Emily Stoll, DR. AP
- Phone Number: +491735697566
- Email: sandraemilystoll@googlemail.com
Study Contact Backup
- Name: Julius D Neubert
- Phone Number: +4915752988296
- Email: jneuber2@smail.uni-koeln.de
Study Locations
-
-
NRW
-
Cologne, NRW, Germany, 50937
- Recruiting
- Department of Anesthesiology and Intensive Care Medicine
-
Contact:
- Sandra E Stoll, MD
- Phone Number: +491735697566
- Email: sandraemilystoll@googlemail.com
-
Contact:
- Sandra E Stoll, MD
- Phone Number: Stoll +491735697566
- Email: sandra-emily.stoll@gmx.de
-
Principal Investigator:
- Sandra E Stoll, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients admitted to an ICU between the years 2005-2023
Exclusion Criteria:
- Patients without ICU admission or ICU admission < 4 hours
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
ICU patients
All ICU patients in different countries worldwide from 2005-2023
|
ICU treatment
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Length of mechanical ventilation
Time Frame: 2024-2040
|
Forecasting mechanical ventilation for the next 16 years
|
2024-2040
|
|
Length of ICU stay
Time Frame: 2024-2040
|
Forecasting ICU stay for the next 16 years
|
2024-2040
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 23-1096-retro
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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