ClinicalTrials.gg
Not yet recruitingNCT07762131Updated Aug 13, 2026

AI-Based Precision Transfusion Prediction Model in Critically Ill Patients

An observational study in Critical Illness, Multiple Organ Dysfunction Syndrome and Blood Transfusion, sponsored by Second Affiliated Hospital, Zhejiang University, School of Medicine. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-13.

Primary conditionMultiple Organ FailureRegistry: Critical IllnessReclassifiedWhy we changed it
Registry
Critical Illness — the first condition term the registry derived for this study.
ClinicalTrials.gg
Multiple Organ Failure
Why
  1. Critical Illness is a broad heading, used only when no more specific condition is named.
  2. The study's listed conditions name Multiple Organ Failure.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Second Affiliated Hospital, Zhejiang University, School of Medicine · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,598
Ages
18 Years and older
Sex
All
01

Study summary

This multicenter observational study aims to develop and validate an artificial intelligence-based precision transfusion prediction model for critically ill patients. The study will collect clinical characteristics, laboratory parameters, transfusion-related information, physiological data, and clinical outcomes from critically ill patients admitted to intensive care units. An AI model will be developed using retrospective data and further evaluated using prospective observational data. The primary objective is to investigate factors associated with multiple organ dysfunction syndrome (MODS) and establish a predictive model to support individualized transfusion management in critically ill patients.

Read the detailed description

Critically ill patients frequently require red blood cell transfusion during intensive care. However, transfusion decisions based solely on conventional indicators may not fully reflect individual differences in disease severity, oxygen delivery, and risk of organ dysfunction. Unnecessary transfusion may increase the risk of adverse outcomes, whereas delayed transfusion may worsen tissue hypoxia.

This multicenter observational study aims to establish an artificial intelligence-based precision transfusion prediction model for critically ill patients. The study includes retrospective model development and prospective observational validation phases.

Clinical data including demographic characteristics, underlying diseases, laboratory parameters, physiological variables, transfusion records, severity scores, organ function indicators, and clinical outcomes will be collected. Machine learning approaches will be applied to identify important predictors associated with multiple organ dysfunction syndrome (MODS) and transfusion-related outcomes.

The developed model will be evaluated based on predictive performance, including discrimination, calibration, and clinical applicability. This study aims to provide an individualized risk assessment approach to improve transfusion decision-making and facilitate precision management in critically ill patients.

02

Conditions studied

  • Critical Illness
  • Multiple Organ Dysfunction Syndrome
  • Blood Transfusion

Browse trials for

Keywords

  • Artificial Intelligence
  • Precision Transfusion
  • Critically Ill Patients
  • Multiple Organ Dysfunction Syndrome
03

In context

Multiple Organ Failure Reclassified

193 studies on the registry are indexed under Multiple Organ Failure; 47 are open to participants now.

This study's planned enrollment of 2,598 is above the median of 200 across 94 observational studies indexed under Multiple Organ Failure.

Browse Multiple Organ Failure studies →

Lead sponsor

Second Affiliated Hospital, Zhejiang University, School of Medicine is the lead sponsor of 99 studies on the registry; 67 are open to participants now.

Compared within Multiple Organ Failure, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Critical Illness. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

This study includes adult critically ill patients admitted to intensive care units. Clinical data including demographic characteristics, underlying diseases, severity indicators, laboratory parameters, transfusion-related information, and clinical outcomes will be collected from electronic medical records. The study population will be used to develop an artificial intelligence-based prediction model for precision transfusion management and risk assessment of multiple organ dysfunction syndrome in critically ill patients.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult patients (aged ≥18 years) admitted to the intensive care unit.
  • Patients with available clinical data, including demographic characteristics, laboratory parameters, transfusion-related information, and clinical outcomes.
  • Patients meeting the requirements for model development and analysis.

Exclusion criteria

Exclusion Criteria:

  • Patients younger than 18 years.
  • Patients with missing key clinical information required for analysis.
  • Patients with repeated ICU admissions during the study period (only the first ICU admission will be included).
  • Patients whose data cannot be used for research purposes according to ethical requirements.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,598 participants (estimated)
Patient registry
No

Groups and cohorts

  • Critically Ill Patient Cohort

    Other: Red Blood Cell Transfusion Exposure

Interventions

  • OtherRed Blood Cell Transfusion Exposure

    Red blood cell transfusion exposure refers to the receipt of red blood cell transfusion during intensive care hospitalization. Transfusion-related information, including transfusion status, number of transfused units, and cumulative transfusion volume, will be collected from routine clinical care records. Transfusion decisions are not assigned by the study protocol, and no intervention is performed as part of this observational study.

06

What researchers measure

Primary outcomes

  1. Occurrence of Multiple Organ Dysfunction Syndrome (MODS)

    The primary outcome is the occurrence of multiple organ dysfunction syndrome (MODS) during intensive care unit hospitalization. MODS will be defined according to clinical diagnostic criteria based on dysfunction of two or more organ systems.

    Time frame: During ICU hospitalization (up to 28 days after ICU admission)

Secondary outcomes

  1. ICU Mortality

    Death occurring during the intensive care unit stay.

    Time frame: Up to Day 28 after ICU admission

  2. Hospital Mortality

    Death occurring during the index hospitalization

    Time frame: Up to Day 28 after ICU admission

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07762131
Lead sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
Responsible party
Sponsor
First posted
Aug 13, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
May 1, 2029 (estimated)
Completion
Sep 1, 2029 (estimated)
Last update
Aug 13, 2026
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion