Actively Recruiting
KIA-Korekt: Staged Unimodal-to-Multimodal AI Evaluation for Perioperative Risk Prediction in Colorectal Cancer
Led by Rene Mantke · Updated on 2026-04-17
910
Participants Needed
1
Research Sites
912 weeks
Total Duration
On this page
Sponsors
R
Rene Mantke
Lead Sponsor
T
Technische Universität Dresden
Collaborating Sponsor
AI-Summary
What this Trial Is About
Perioperative complications following surgery for colorectal cancer (CRC) represent a major cause of postoperative morbidity and mortality. Existing risk stratification tools lack the precision to capture the complex biological and morphological factors that determine individual patient vulnerability. Artificial intelligence (AI)-based analysis of medical imaging data offers a promising approach to improve preoperative risk prediction. The KIA-Korekt study investigates whether perioperative complications in CRC patients can be predicted using multimodal AI-based image analysis. Three complementary imaging modalities are integrated: digital histopathology (haematoxylin-eosin whole-slide images, H\&E-WSIs), preoperative CT and MRI radiomics, and multiplex tissue imaging (mTI) including multiplex immunohistochemistry (mIHC) and imaging mass cytometry (IMC). The study includes a retrospective cohort of approximately 750 CRC patients treated between 2011 and 2021, and a prospective validation cohort of approximately 210 patients recruited from 2026 to 2028. Deep learning and radiomic feature extraction pipelines are applied to all modalities individually and in multimodal combination. Predicted outcomes include anastomotic leakage, wound infection, sepsis, ICU admission, and in-hospital mortality within 30 days of surgery. The study is conducted at the University Hospital Brandenburg, Brandenburg Medical School Theodor Fontane, in collaboration with the Department of Computational Pathology, TU Dresden.
CONDITIONS
Official Title
KIA-Korekt: Staged Unimodal-to-Multimodal AI Evaluation for Perioperative Risk Prediction in Colorectal Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients (≥18 years)
- Histologically confirmed colorectal adenocarcinoma
- Undergoing surgical resection (curative or palliative intent)
- Availability of H&E-stained whole-slide images (WSIs) from the primary tumour
You will not qualify if you...
- Patients not undergoing surgical treatment
- Missing H&E-stained tissue slides of the primary tumour
- Histopathological material of insufficient quality for analysis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital Brandenburg an der Havel, Brandenburg an der Havel, Germany (Single-center)
Brandenburg an der Havel, Germany
Actively Recruiting
Research Team
M
Melissa Horner, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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