MedDataX Logo

Database for Predicting Clinical Outcomes of Critically Ill Patients

NCT ID: NCT04541849

Last Updated: 2024-05-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

20000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-09-10

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Australian and New Zealand Intensive Care Society (ANZICS) has built a Center of Outcome and Resource Evaluation (CORE) adult patients database (APD) of adult critically ill patients. ANZICS CORE APD has built an international collaboration of ICU database. National Taiwan University Hospital has joined this international collaboration and built the data according to the APD data dictionary with same value domain attributes and data element attributes. We retrospectively collected the data of patients discharged from the March 1, 2019 to June 30, 2022. Data of this database are permitted to study clinical problems and predict the clinical outcomes of these critically ill patients using statistical methods and machine learning techniques.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Adult Intensive Care Units Database of National Taiwan University Hospital

NCT04541862

Critical Illness
RECRUITING

Taiwan Center of Outcome and Resource Evaluation

NCT04875260

Critical Illness
RECRUITING

The Blood Pressure Analysis on Critically Ill Patients

NCT03827369

Multiple Organ Failure Intensive Care Unit Syndrome
UNKNOWN

Adrenal Exhaustion Syndrome in Critically Ill Patients Without Improvement

NCT00674284

Survival
COMPLETED

Acute Respiratory Distress Syndrome in Taiwan

NCT03260348

Acute Respiratory Distress Syndrome
UNKNOWN

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Data of this database are permitted to study the following clinical issues: including delirium, sepsis, acute kidney injury, acute respiratory distress syndrome, disseminated intravascular coagulation, multiple organ injuries, nutrition, survival status, number of days on ventilators, need for renal replacement therapy, length of stays in intensive care unit, length of stay in hospital, and other relevant clinical outcomes. It is also planned to analyze the clinical prognosis of special disease subgroups and establish a prediction model according to the type of patient's disease.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Critical Illness

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Critically ill patients

Critical Care

Intervention Type OTHER

Critical care in the intensive care units

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Critical Care

Critical care in the intensive care units

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Critically ill patients admitted to intensive care units

Exclusion Criteria

* patients aged less than 18 years
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

National Taiwan University Hospital

Taipei, , Taiwan

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Taiwan

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Yu-Chang Yeh, MD, PhD

Role: CONTACT

[email protected]
+886-9-10513711

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Yu-Chang Yeh, MD, PhD

Role: primary

[email protected]
+886-910513711

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

202004016RINB

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Establish a Prospective Registration System of ARDS Patients for Improving Quality of Care
NCT04032288 COMPLETED
Characteristics of Critically Ill Patients With Severe Acute Respiratory Syndrome Coronavirus 2 Infection (COVID-19)
NCT04948242 UNKNOWN
Development of a Biological Database in the Field of Operative Intensive Care
NCT03014427 RECRUITING
Research on Risk Assessment and Early Warning Models for Adverse Clinical Outcomes in Critically Ill Patients
NCT07317817 COMPLETED
The Prognostic Factors of COVID-19 ARDS Patients and Their Long-term Follow-up of Pulmonary Function Test
NCT05490914 UNKNOWN
The PREDICT Study- a Registry in Critically Ill Patients to Determine Predictors of Disability Free Survival
NCT03226912 COMPLETED
Assessment of Microcirculation Alteration With Both Sublingual Microcirculation and Near-infrared Spectroscopy on ARDS
NCT05180409 UNKNOWN
Serial Changes of Soluble Triggering Receptor Expressed on Myeloid Cells-1 (sTREM-1) Levels in Patients With Acute Respiratory Distress Syndrome
NCT00557414 COMPLETED
Prediction of Safe Discharge From ICU
NCT05459350 COMPLETED
Microcirculation and Oxidative Stress in Critical Ill Patients in Surgical Intensive Care Unit
NCT00808691 COMPLETED
The IndONEsia ICCU Registry: a Multicenter Cohort of Intensive Cardiovascular Care Units Patients in Indonesia
NCT06265714 COMPLETED
The Early Prediction of Sepsis in ICU
NCT05088850 UNKNOWN
Clinical Features, Treatments, and Outcomes in Acute Respiratory Distress Syndrome (ARDS-CTO)
NCT07186140 NOT_YET_RECRUITING
Anti-pyretic Therapy in Critically Ill Adults
NCT01173367 COMPLETED PHASE2
Study of Biomarkers in Patients of Sepsis Complicated With Acute Respiratory Distress Syndrome (ARDS)
NCT04552821 UNKNOWN
Prediction Study of Complications After Severe Trauma
NCT01713205 UNKNOWN
Assessment of OHIR Score to Predict a Prolonged Intensive Care Unit Stay
NCT02945358 COMPLETED
Serum STREM and MNDA Mointoring in ICU
NCT02120521 COMPLETED
PDMS Outcome After Intensive Care, Organdysfunction and Monitoring
NCT03379688 COMPLETED
Outcome Factors of Pneumonia Patients in Critical Care Unit
NCT05899192 NOT_YET_RECRUITING
Evaluation of the Association Between Day and Time of Admission to Critical Care and Acute Hospital Outcome
NCT02751164 COMPLETED
The Relationship Between Positive End Expiratory Pressure and Cardiac Index in Patients With Acute Respiratory Distress Syndrome (ARDS) Managed on a Fluid Protocol
NCT01714583 COMPLETED
Machine Learning Prediction of Parameters of Early Warning Scores in Intensive Care Units
NCT06259812 ACTIVE_NOT_RECRUITING
A Feasibility Study to Assess Pre Admission Status and Six Month Outcomes After Major Trauma
NCT02917694 COMPLETED
Multimodal Database and Large Language Model for ARDS
NCT06973733 NOT_YET_RECRUITING