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OncoMatch/Clinical Trials/NCT06435286

Effectiveness and Performance of an Optical Biopsy Technology for Esophageal Cancer in Brazil and the United States

Is NCT06435286 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Proflavine Hemisulfate and Artificial Intelligence Mobile High-Resolution Microendoscope for suspected or known squamous cell neoplasia.

Phase 2RecruitingBaylor College of MedicineNCT06435286Data as of May 2026

Treatment: Proflavine Hemisulfate · Artificial Intelligence Mobile High-Resolution MicroendoscopeIn a previous clinical trial in China and the United States (US), the investigators developed and validated a mobile, high-resolution microendoscope (mHRME) for screening and surveillance of esophageal squamous cell neoplasia (ESCN). The trial revealed higher specificity for qualitative (visual) interpretation by experts but not the novice and in the surveillance arm (100% vs. 19%, p \<0.05). In the screening arm, diagnostic yield (neoplastic biopsies/total biopsies) increased 3.6 times (8 to 29%); 16% of patients were correctly spared any biopsy, and 18% had a change in clinical plan. In a pilot study in Brazil, the investigators tested a software-assisted mHRME with deep-learning software algorithms to aid in the detection of neoplastic images and determine the performance, efficiency, and impact of the AI-mHRME when to Lugol's chromoendoscopy (LCE) alone and when using AI-mHRME with LCE. In this clinical trial, the investigators will build on the Brazil pilot trial data to optimize an artificial intelligence (AI) mHRME and evaluate its clinical impact and implementation potential in ethnically and socioeconomically diverse populations in the US and Brazil.

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Extracted eligibility criteria

Disease stage

Excluded: Stage ADVANCED SQUAMOUS CELL CARCINOMA OF THE DISTAL ESOPHAGUS

Known advanced squamous cell carcinoma of the distal esophagus or dysplastic/suspected malignant esophageal lesion greater than or equal to 2 cm in size not amenable to endoscopic therapy [excluded]

Lab requirements

Blood counts

Prothrombin time greater than 50% of control; PTT greater than 50 sec, or INR greater than 2.0 [excluded]

Prothrombin time greater than 50% of control; PTT greater than 50 sec, or INR greater than 2.0 [excluded]. Inability to tolerate sedated upper endoscopy due to cardio-pulmonary instability or other significant medical issues [excluded].

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Baylor St. Luke's Medical Center · Houston, Texas
  • Ben Taub Hospital (Harris Health Systems) · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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