NCT07495527

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2026

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 20, 2026

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

March 21, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 27, 2026

Completed
Last Updated

March 27, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

March 21, 2026

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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)

Location

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: 39012345BACKGROUND
  • Wanchaijiraboon 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: 36851234BACKGROUND
  • Gonzalez 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

Hip Fractures

Condition Hierarchy (Ancestors)

Femoral FracturesFractures, BoneWounds and InjuriesHip InjuriesLeg Injuries

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

Locations