Clinical Data-Driven AI Model for Mortality Prediction After Hip Fracture
Development of an AI Model Based on Clinical Data to Predict 30-Day and 1-Year Mortality Rates After Hip Fracture Surgery: A Retrospective Cohort Study
1 other identifier
observational
1,000
1 country
1
Brief Summary
Hip fractures are a major cause of morbidity and mortality, particularly in elderly patients. Accurate prediction of postoperative mortality is critical for risk stratification and clinical decision-making. Traditional scoring systems, such as the Nottingham Hip Fracture Score, have limitations in capturing complex, non-linear relationships among clinical variables. This retrospective cohort study aims to develop and validate an artificial intelligence-based model to predict 30-day mortality in patients undergoing hip fracture surgery. Clinical and laboratory data of approximately 1000 patients operated between January 1, 2022 and December 1, 2025 will be extracted from electronic health records. Variables include demographic characteristics, comorbidities, laboratory parameters, perioperative data, and postoperative complications. The performance of the artificial intelligence model will be evaluated and compared with conventional risk scoring systems. The study seeks to determine whether AI-based approaches can provide improved predictive accuracy for postoperative mortality in hip fracture patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 20, 2026
CompletedFirst Submitted
Initial submission to the registry
March 21, 2026
CompletedFirst Posted
Study publicly available on registry
March 27, 2026
CompletedMarch 27, 2026
March 1, 2026
3 months
March 21, 2026
March 21, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
30-Day Postoperative Mortality
All-cause mortality occurring within 30 days following hip fracture surgery, determined from hospital records and electronic health data.
30 days after surgery and 1 year later
Eligibility Criteria
This study population consists of adult patients who underwent surgical treatment for hip fractures at a tertiary care oncology training and research hospital between January 1, 2022 and December 1, 2025. The cohort is derived retrospectively from electronic health records and includes approximately 1000 patients. The population includes individuals with varying demographic characteristics, comorbidities, and perioperative risk profiles. Clinical data encompass demographic information, baseline functional and cognitive status, comorbid conditions, laboratory parameters, intraoperative variables, and postoperative complications. Patients with malignancy and those undergoing revision surgery are excluded. The study population represents a real-world clinical cohort used to develop and validate an artificial intelligence-based model for predicting 30-day postoperative mortality following hip fracture surgery.
You may qualify if:
- Patients who underwent surgical treatment for hip fracture between January 1, 2022 and December 1, 2025 Age ≥18 years Availability of complete demographic, clinical, and laboratory data in the electronic health record system Documented 30-day follow-up or mortality status
You may not qualify if:
- Patients with malignancy Patients undergoing revision hip surgery Patients with missing or incomplete key clinical or laboratory data required for analysis Patients with unavailable or undocumented 30-day mortality status
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Ankara, 06200, Turkey (Türkiye)
Related Publications (3)
Ju M, Lee S, Marvich HM, Lin S. Accessing Alkoxy Radicals via Frustrated Radical Pairs: Diverse Oxidative Functionalizations of Tertiary Alcohols. J Am Chem Soc. 2024 Jul 24;146(29):19696-19703. doi: 10.1021/jacs.4c07125. Epub 2024 Jul 16.
PMID: 39012345BACKGROUNDWanchaijiraboon P, Sainamthip P, Teeyapun N, Luangdilok S, Poovorawan Y, Wanlapakorn N, Tanasanvimon S, Sriuranpong V, Susiriwatananont T, Zungsontiporn N, Pakvisal N. Safety Following COVID-19 Booster Vaccine with BNT162b2 Compared to mRNA-1273 in Solid Cancer Patients Previously Vaccinated with ChAdOx1 or CoronaVac. Vaccines (Basel). 2023 Feb 3;11(2):356. doi: 10.3390/vaccines11020356.
PMID: 36851234BACKGROUNDGonzalez Martinez J, Chen JJ, Aung T, Constantine T, Gonzalez-Martinez JA. Comparative Feasibility and Complication Analyses of Extraoperative (Bedside) Removal of Stereo-Electroencephalography Electrodes. Stereotact Funct Neurosurg. 2025;103(5):302-311. doi: 10.1159/000545984. Epub 2025 Apr 23.
PMID: 40267891BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- M.D
Study Record Dates
First Submitted
March 21, 2026
First Posted
March 27, 2026
Study Start
December 1, 2025
Primary Completion
March 10, 2026
Study Completion
March 20, 2026
Last Updated
March 27, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to the retrospective nature of the study and the inclusion of sensitive patient information obtained from electronic health records. All data will be analyzed in an anonymized form, and data sharing is restricted in accordance with institutional policies and ethical regulations