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Copyright: ©Author(s) 2026.
World J Gastrointest Endosc. Nov 16, 2026; 18(11): 126153
Published online Nov 16, 2026. doi: 10.4253/wjge.126153
Table 2 Representative clinical and diagnostic-validation studies of artificial intelligence across gastrointestinal endoscopy tasks and workflows
Ref.
Region/setting
Population/sample size
AI function
Study design/comparator
Evaluation unit
Key findings
Validation/main limitation
Wang et al[7], 2019China; colonoscopy1058 patients; 522 CADe, 536 controlReal-time CADeProspective randomized trial; CADe vs standard colonoscopyPatientADR: 29.1% vs 20.3%; adenomas/patient: 0.53 vs 0.31Single-center, non-blinded trial; benefit mainly driven by diminutive adenomas
Byrne et al[8], 2019Colonoscopy video125 diminutive-polyp videos; 106 analyzedCADx for adenoma vs hyperplastic polypIndependent video test set; histopathology referenceLesion/videoSensitivity: 98%; specificity: 83%; accuracy: 94%; NPV: 97%Offline video evaluation; 19/125 lesions lacked sufficient prediction confidence; no live clinical trial
Wu et al[9], 2019China; EGD324 randomized; 303 analyzedWISENSE blind-spot monitoringRCT; WISENSE-assisted vs conventional EGDPatient/procedureBlind spot rate: 5.86% vs 22.46%, P < 0.001Single-center trial; procedure-quality endpoint
Gong et al[23], 2020China; colonoscopy704 randomized; 355 ENDOANGEL, 349 controlReal-time CADe/withdrawal-quality supportRandomized trial; ENDOANGEL vs unassisted colonoscopyPatientADR: 16% vs 8%; odds ratio: 2.3, P = 0.001Single-center study; relatively low baseline ADR
Wang et al[24], 2020China; colonoscopy1010 randomized; 962 analyzedReal-time CADeDouble-blind randomized trial; CADe vs sham systemPatientADR: 34% vs 28%; odds ratio: 1.36, P = 0.03Single-center; interval-CRC benefit not evaluated
Repici et al[25], 2020Italy; colonoscopy685 participants; 341 CADe, 344 controlGI Genius CADeMulticenter randomized trial; CADe vs standard colonoscopyPatient/procedureADR: 54.8% vs 40.4%; APC: 1.07 vs 0.71Multicenter clinical evidence; no long-term cancer-outcome assessment
Shaukat et al[26], 2022United States; screening/surveillance colonoscopy1359 analyzed; 682 CADe, 677 standardSKOUT CADeMulticenter randomized trial; CADe vs standard colonoscopyPatient/procedureADR: 47.8% vs 43.9%, P = 0.065; APC: 1.05 vs 0.83, P = 0.002Multicenter United States evidence; ADR difference not statistically significant
Spada et al[36], 202414 European centers; small-bowel CE137 enrolled; 133 analyzedAI-assisted capsule readingProspective multicenter paired comparison; AI-assisted vs standard readingPatientDiagnostic yield: 73.7% vs 62.4%; reading time: 3.8 minutes vs 33.7 minutesStrong workflow benefit; downstream management and clinical outcomes not evaluated
Seager et al[27], 2024United Kingdom; 12 NHS hospitals2032 randomizedGI Genius CADePragmatic multicenter RCT; CADe vs standard colonoscopyPatient/procedureAdenomas/procedure: 1.56 vs 1.21; ADR: 56.6% vs 48.4%Strong routine-practice evidence; open-label design
Maas et al[28], 2024Europe/Canada; 7 centers581 enrolled; 497 analyzedCADeInternational randomized trial; CADe vs conventional colonoscopyPatient/procedureADR: 38.4% vs 37.7%; APC: 0.66 vs 0.66Experienced endoscopists; not statistically significant
Yao et al[47], 2024China; screening colonoscopy393 patientsAI bowel-preparation assessmentProspective observational validation; AI e-BBPS with tandem colonoscopy outcome assessmentPatient/procedure> 5-mm AMR: 35.71% in unqualified-AI vs 13.19% in qualified-AISingle-center observational study; no randomized AI-vs-standard intervention


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