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RECRUITING NA

Investigation of Standard Excision Surgical Margins Using Two Photon Fluorescence Microscopy

NCT06473103 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to compare the use of two photon fluorescence microscopy for detecting residual basal cell carcinoma during standard local excision.

Conditions Studied

Interventions

  • DEVICE Two photon fluorescence microscopy imaging

Study Locations (1)

New York

  • Rochester Dermatologic Surgery — Victor

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2024-10-29
Est. Completion 2026-04
Phase NA

Sponsor

University of Rochester

437 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06473103

The ClinicalTrials.gov registry entry for NCT06473103 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 437 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Basal Cell Carcinoma appearing as the primary indexed condition, and to 1 intervention — of which Two photon fluorescence microscopy imaging is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06473103 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06473103 about?

NCT06473103 is a clinical study titled "Investigation of Standard Excision Surgical Margins Using Two Photon Fluorescence Microscopy". The goal of this clinical trial is to compare the use of two photon fluorescence microscopy for detecting residual basal cell carcinoma during standard local excision.

What is the current status of trial NCT06473103?

This trial is currently recruiting. It is a NA study. The enrollment target is 52 participants. The study started on 2024-10-29. Estimated completion is 2026-04.

What conditions does trial NCT06473103 study?

This clinical trial studies the following conditions: Basal Cell Carcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06473103?

The interventions under investigation include: Two photon fluorescence microscopy imaging (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06473103?

This trial is sponsored by University of Rochester, which has 437 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06473103 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial