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RecruitingNCT06791447Updated Apr 17, 2025

AI-Driven Prediction of Dialysis Outcome With EHR

An observational study in Dialysis Patients, sponsored by The Eye Hospital of Wenzhou Medical University. Recruiting at 1 site in China. Open to participants aged 20 Years to 100 Years. Per ClinicalTrials.gov, last updated 2025-04-17.

Sponsored by The Eye Hospital of Wenzhou Medical University · Observational

From the registry’s dates

  • Primary completion was expected by May 2025, 1 year 5 months ago, but the record still lists the study as recruiting.
  • Started Jan 2023; still recruiting 3 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,000,000
Ages
20 Years to 100 Years
Sex
All
01

Study summary

This is a multi-center, clinical study designed to evaluate the application and effectiveness of an AI-assisted predictive model for outcome of dialysis patients, leveraging multimodal health data.

Read the detailed description

This study aims to develop an AI-assisted model to predict clinical outcomes in dialysis patients, focusing on both primary outcomes (e.g., mortality) and intermediate outcomes (e.g., anemia, blood pressure, nutritional status, and calcium-phosphate metabolism). The study will utilize patients' EHR data, including laboratory test results, medical history, dialysis treatment information, and clinical observations, to predict these health outcomes. The goal is to improve early identification of at-risk patients, enabling better clinical decision-making and personalized care strategies.

02

Conditions studied

  • Dialysis Patients

Keywords

  • Dialysis Patients
  • AI-Assisted Prediction
03

In context

Lead sponsor

The Eye Hospital of Wenzhou Medical University is the lead sponsor of 15 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of dialysis patients from the China Hemodialysis National Network Center, which includes a wide range of patients undergoing hemodialysis treatment at participating hospitals across China. Participants will be selected based on the availability of comprehensive electronic health records (EHR), including medical history, laboratory test results, dialysis treatment details, and clinical observations. The cohort will include both male and female patients, with varying degrees of health status, including those with comorbidities commonly associated with dialysis. The study aims to utilize this diverse group to assess and predict outcomes related to mortality and complications in dialysis patients.

Inclusion criteria

  1. Patients who have been undergoing dialysis (either hemodialysis or peritoneal dialysis) for at least 3 months.
  2. Complete and accessible EHR data, including medical history, laboratory test results, dialysis treatment details, and clinical observations.
  3. Participants must provide informed consent for the use of their health data for research purposes.

Exclusion criteria

Exclusion Criteria:

  1. Patients with incomplete or missing critical EHR data, including medical history, laboratory results, dialysis data, or treatment details necessary for the study.
  2. Patients who have been on dialysis for less than 3 months, to ensure stable data for outcome prediction.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,000,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • High Risk Group

    Participants predicted to have a high risk of mortality based on AI-assisted prediction models using their EHR data, including medical history, lab results, dialysis treatment details, and clinical observations.

    Other: AI-assisted Predictive Model for Dialysis Outcomes

  • Low Risk Group

    Participants predicted to have a low risk of mortality based on the AI-assisted prediction model, who will be compared with the high-risk group for evaluating the effectiveness of early intervention strategies.

    Other: AI-assisted Predictive Model for Dialysis Outcomes

Interventions

  • OtherAI-assisted Predictive Model for Dialysis Outcomes

    This study utilizes an AI-assisted predictive model that analyzes multimodal data from electronic health records, including medical history, laboratory results, dialysis treatment details, and clinical observations, to predict outcomes for dialysis patients. The model employs deep learning algorithms to predict mortality risk, intermediate outcomes such as anemia, blood pressure control, nutrition, and calcium-phosphate metabolism, and helps identify early signs of deterioration. The intervention is not a direct treatment or procedure but aims to develop a tool for predicting patient outcomes and optimizing treatment strategies to improve overall health and survival rates for dialysis patients.

06

What researchers measure

Primary outcomes

  1. Mortality Prediction Accuracy

    The ability of the AI-assisted predictive model to accurately predict the risk of mortality in dialysis patients. Prediction accuracy will be assessed using the Area Under the Curve (AUC), F1 score, and sensitivity/specificity. The model will be evaluated by comparing the predicted mortality risk with actual outcomes (i.e., whether patients survived or passed away during the study period).

    Time frame: 1 year

Secondary outcomes

  1. Complications Prediction Accuracy

    The accuracy of the AI-assisted predictive model in forecasting complications commonly experienced by dialysis patients, including anemia, uncontrolled blood pressure, poor nutritional status, and abnormalities in calcium-phosphate metabolism. The model's performance will be assessed using metrics such as AUC, F1 score, and accuracy by comparing predicted values to actual clinical outcomes, such as lab results, clinical diagnoses, and patient health status.

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • General Hospital of PLA
    Beijing, Beijing, China
    Recruiting
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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 Apr 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06791447
Lead sponsor
The Eye Hospital of Wenzhou Medical University
Responsible party
Kang Zhang (Chief Scientist, Wenzhou Medical University) — Principal investigator
First posted
Jan 24, 2025
Start date
Jan 1, 2023
Primary completion
May 2025 (estimated)
Completion
May 1, 2025 (estimated)
Last update
Apr 17, 2025

Study contacts

Fei Liu, MD
Contact
liufei_2359@163.com
+86 13810512704

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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