The Diagnostic Accuracy of the Device Under Development MULTISCOPE

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS

About this trial

Conventional gastrointestinal endoscopy relies on ex vivo histopathology, a process limited by diagnostic delays and high costs. The MULTISCOPE project introduces a miniaturized (2.2 mm) endoscopic device integrating advanced optical biopsy with Cold Argon Plasma (CAP) therapy. Utilizing multimodal optical fibers, the system performs label-free, high-resolution imaging via two-photon autofluorescence and second-harmonic generation.

Simultaneously, the integrated CAP technology enables targeted oncological treatment by inducing apoptosis and cell-cycle arrest with minimal collateral damage. Given that Endoscopic Submucosal Dissection (ESD) inherently provides samples containing both neoplastic and healthy margins (5-8 mm safety zone), this platform allows for precise, real-time tissue characterization. This in vitro pilot study evaluates the system's diagnostic accuracy in discriminating between healthy and neoplastic colorectal tissues.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Colonic or rectal neoplastic lesions resectable by endoscopic submucosal dissection (ESD)

Age ≥ 18 years, male and female

patients with American Society of Anesthesiologists (ASA) grades 1-3

Signed informed consent

Disqualifiers

Severe medical comorbidities precluding endoscopy;

Uncontrolled coagulopathy;

Pregnancy or planned pregnancy during the period of study participation;

Life expectancy ≤2 years, as judged by the site investigator;

Trial design

Design model

Single group

Treatments tested in this trial

  • endoscopic submucosal dissection (ESD)

    Procedure/Surgery

    Protocol and Transport Colorectal ESD specimens will be resected at the Fondazione Gemelli IRCCS and immediately transported dry (without formalin) to the UCSC Pathological Anatomy Unit within 15 minutes. To ensure tissue viability, dedicated staff will coordinate the transfer directly from the endoscopy suite. Ex Vivo Analysis The MULTISCOPE device will be stationed at the UCSC facility, adjacent to the pathology lab. Upon arrival, Prof. Vincenzo Arena's team will perform multimodal fiberoptic optical biopsies on both healthy and neoplastic mucosa before proceeding with standard histopathological processing.

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Patients who require endoscopy with endoscopic submucosal dissection (ESD) of the colon.Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Diagnostic Accuracy (Area Under the ROC Curve [AUC]) of the MULTISCOPE Device for Differentiating Normal versus Neoplastic Colorectal Tissue

The diagnostic accuracy of optical biopsies performed with the two-photon microendoscope MULTISCOPE prototype will be assessed and compared against standard ex vivo histopathology (gold standard) as the reference diagnosis. Diagnostic performance will be evaluated based on the Area Under the Receiver Operating Characteristic Curve (AUC). Optimal sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) with 95% confidence intervals will also be calculated using the Youden Index threshold. AUC values range from 0.5 (no discrimination) to 1.0 (perfect diagnostic accuracy).

Time frame
At the time of histopathological evaluation, approximately 2 weeks after the surgical procedure.

Secondary outcomes

1

Tumor Cell Destruction Rate After Cold Atmospheric Plasma (CAP) Exposure

The therapeutic efficacy of MULTISCOPE expressed as the proportion of treated/affected cells after CAP exposure, quantified in commercial gastrointestinal tumor organoids.

Time frame
Up to 12 months (at the end of the study).

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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