Image

Utility and Usability of ActivSight™ Laser Speckle Imaging in Visualization of Tissue Perfusion and Blood Flow During Esophageal Surgery in Humans

Utility and Usability of ActivSight™ Laser Speckle Imaging in Visualization of Tissue Perfusion and Blood Flow During Esophageal Surgery in Humans

Recruiting
18 years and older
All
Phase N/A

Powered by AI

Overview

ActivSight™ combines an innovative form factor and proprietary software to deliver precise, objective, real-time visualization of blood flow and tissue perfusion intraoperatively for laparoscope-based surgery. A small adaptor that fits between any existing laparoscope and camera systems and a separate light source placed along any current commercial system will deliver objective real-time tissue perfusion and blood flow information intraoperatively.

Primary Objective: To determine the feasibility of ActivSight™ in detecting and displaying tissue perfusion and blood flow in the conduit and foregut anastomoses in esophageal resection/reconstructive surgery. The investigators will compare the precision and accuracy among the naked eye inspection, ICG and LSCI in assessing the vascularity of the conduit.

Description

Design
  • This is a prospective interventional cross-over study where ActivSight™ will be used in sequence to the standard practice of visualizing perfusion status of the conduit using the naked eye visual inspection and ICG during esophageal resection.
  • Feasibility will be determined by technically successful completion of intended visualization.
  • Safety will be determined through clinical assessments and evaluation of any adverse event.
  • Assessment of preliminary efficacy will be performed through analysis of any intraoperative decisions made based on visual display as compared to standard endoscopic approach, or non-inferiority to ICG-based visualization and usability.
  • Patient outcome and follow up to Postoperative day 28 will be monitored for clinical outcome.
  • Target enrollment for the assessment of esophageal anastomoses is a total of seventy patients powered to detect ~ 2-3 cm discordance between ICG and LSCI lines of demarcation between well vascularized and less vascularized sites in the gastric conduit. Since ActivSight™ can detect the difference of > 2 cm between perfused versus less perfused in comparison to ICG with 80 % confidence at p<0.05 in a sample size of n
    • 21, the investigators estimate that the study will require an accrual of 63 patients. With potential unforeseen dropout and mortality, the investigators will recruit a total of 70 patients for the proposed study.

Eligibility

INCLUSION CRITERIA

        All patients age > 18 years old undergoing laparoscopic esophageal resection and
        reconstruction surgery; spoken command and literacy in the native language spoken at each
        participating center; ability to understand and follow study procedures; and having
        provided signed consent.
        Diagnosis:
          -  All patients with a clinical suspicion and diagnosis of benign or malignant, small or
             large bowel lesions requiring surgical resection.
          -  Typical imaging as per standard workup findings including US, CT and/or MRI. Plain
             radiographs and contrast imaging may be obtained by referring physicians and are
             helpful for confirming the clinical diagnosis.
        Location of pathology or resected segment:
        * Target lesions can be located in any fore-, mid- or hindgut segments requiring
        reconstruction and anastomoses.
        Prior therapy:
        * Patients with prior surgery are eligible for enrollment.
        Laboratory:
          -  Hemoglobin > 9 g/dL
          -  Platelet count ≥75,000/µL (may receive transfusions)
          -  Normal PT, PTT and INR < 1.5 x ULN (including patients on prophylactic
             anticoagulation)
          -  Renal function: Age-adjusted normal serum creatinine derived from Schwartz formula for
             estimating GFR by the CDC OR a creatinine clearance ≥60 mL/min/1.73 m2 for safe
          -  Adequate pulmonary function: Defined as no dyspnea at rest, and a pulse oximetry >94%
             on room air if there is clinical indication for determination.
        EXCLUSION CRITERIA
          -  There is no exclusion criteria for ActivSightTM for esophageal surgery.
          -  Patients assigned to FDA cleared ICG-based visualization are contraindicated for any
             chronic renal dysfunction, potential drug interaction, history of allergy to ICG or
             anaphylaxis, known allergy to iodides, breast-feeding or being of reproductive age
             with pregnancy possible and not ruled out, and pregnancy.
          -  Patients currently in any investigational agents.

Study details
    Esophagus Cancer
    Esophageal Cancer
    Esophageal Neoplasms
    Esophageal Diseases
    Esophageal Adenocarcinoma
    Esophageal Squamous Cell Carcinoma
    Esophagus SCC
    Esophagus Tumor
    Esophagus Adenocarcinoma
    Esophagus Neoplasm

NCT05591053

Activ Surgical

14 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.