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RecruitingObservational

Microendoscopic Electrical Impedance Sensing for Real-time Intraoperative Surgical Margin Assessment

NCT ID: NCT06039085Sponsor: Ryan J. HalterLast updated: 2026-04-07

Summary

This research will study a custom device developed to detect if any prostate cancer tissue is left behind when the prostate is removed. This device is called an Electrical Impedance Imaging (EII) probe.

Detailed description

Two hundred men will be recruited to participate in this trial. Consent will be obtained from all participating men prior to surgery. The trial will consist of recording EII data from: 1. In vivo pelvic floor and peri-prostatic tissues remaining after the prostate has been resected 2. Resected ex vivo prostate following extraction from the abdomen (in the OR) 3. Resected ex vivo prostate when transferred to Pathology, post-RARP The study team will also track post-surgical complications due to the study's technology (e.g., infection) and additional time required to deploy the study technology used to assess feasibility of clinical integration of the EII device. Post-RARP pathological assessment of margin tissues will be used to train and evaluate the study's classification schemes for identifying Positive Surgical Margin (PSMs).

Arms & interventions

  • Devicecustom device to demonstrate a significant difference in electrical impedance signatures

    Custom device will be used to measure electrical impedance signatures.

Outcome measures

Primary

  • Electrical impedance difference between positive and negative surgical margins

    Outcome measures will include how significantly different electrical impedance signatures are between impedance recordings of positive and negative surgical margins as acquired during prostate surgery.

    Time frame: 2023-2025

Secondary

  • Safety of EI sensing in vivo electrical sensing

    Time frame: 2023-2025

  • Efficacy of EI sensing in vivo electrical sensing

    Time frame: 2023-2025

Eligibility criteria

Sex: MaleAge: 18 Years and olderHealthy volunteers: No
Inclusion Criteria: 1. Clinical diagnosis of prostate cancer requiring RARP. 2. Ability to understand and the willingness to sign a written informed consent document. 3. Age ≥ 18 years old Exclusion Criteria: 1. Adults with implanted electrical devices such as pacemakers 2. Prisoners 3. Adults with impaired decision-making capacity 4. Any condition for which, in the opinion of the investigator, contraindicates study participation.

Study locations (1)

Dartmouth-Hitchcock Medical Center

Lebanon, New Hampshire, 03756

Recruiting
Lawrence M Dagrosa, MD · Contact
Einar Sverrisson, MD · Sub Investigator
Microendoscopic EI Sensing for Real-time Intraoperative Surgical Margin Assessment | Cancerify