RECRUITING

Feasibility of Timesaving When Using Histolog Confocal Laser Endomicroscopy for Margin Assessment in Prostatectomy Specimen

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study investigates a new, faster way to find cancer cells on the surface of the prostate during radical prostatectomy surgery. A recently FDA-approved device, called the Histolog Scanner, gives high-resolution imaging of the surface of fresh tissue using ultra-fast confocal microscopy, which allows physicians to make surgical decisions quickly.

Official Title

Feasibility of Timesaving When Using Histolog Confocal Laser Endomicroscopy for Margin Assessment in Prostatectomy Specimen

Quick Facts

Study Start:2025-05-13
Study Completion:2026-05-13
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07141121

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Localized or locally advanced prostate cancer D'Amico intermediate or high-risk disease.
  2. * Indicated for robot-assisted radical prostatectomy
  3. * Treatment naive.
  4. * Age ≥ 18 years.
  5. * Ability to understand and the willingness to sign a written informed consent.
  1. * Patients who have received pelvic radiation previously for prostate cancer or any other malignancy.
  2. * Patients who have previously received androgen deprivation or other hormonal treatments, or focal therapy of prostate cancer prior to radical prostatectomy.
  3. * Patients with D'Amico Criteria low risk prostate cancer.

Contacts and Locations

Study Contact

Monali Fatterpekar, PhD
CONTACT
(347) 675-8024
monali.fatterpekar@mountsinai.org
Henry W. Jodka, BA
CONTACT
203-939-5115
henry.jodka@mountsinai.org

Principal Investigator

Ashutosh K. Tewari, MD
PRINCIPAL_INVESTIGATOR
Icahn School of Medicine at Mount Sinai

Study Locations (Sites)

Icahn School of Medicine at Mount Sinai
New York, New York, 10029
United States

Collaborators and Investigators

Sponsor: Icahn School of Medicine at Mount Sinai

  • Ashutosh K. Tewari, MD, PRINCIPAL_INVESTIGATOR, Icahn School of Medicine at Mount Sinai

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-13
Study Completion Date2026-05-13

Study Record Updates

Study Start Date2025-05-13
Study Completion Date2026-05-13

Terms related to this study

Keywords Provided by Researchers

  • Confocal Microscopy
  • Histolog Scanner
  • NeuroSafe
  • Surgical Margins
  • Feasibility
  • Radical Prostatectomy

Additional Relevant MeSH Terms

  • Prostate Cancer