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NCT05645523 · ClinicalTrials.gov registry record · Early Phase 1

Indocyanine Green (ICG) Guided Sentinel Lymph Node Mapping for Pediatric Visceral Solid Tumors

A Early Phase 1 study of Solid Tumor, sponsored by St. Jude Children's Research Hospital.

Recruiting
Registry status
Early Phase 1
Development phase
25
Enrollment target
3
Study locations

NCT05645523 is a Early Phase 1 study of Solid Tumor that is actively recruiting participants, run by St. Jude Children's Research Hospital. The registered enrollment target is 25 participants, below the 222-participant average among 196 other Solid Tumor trials with a reported enrollment target (89% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT05645523, a Early Phase 1 study of Solid Tumor, is actively recruiting participants, sponsored by St. Jude Children's Research Hospital.

RECRUITING
Registry status
Early Phase 1
Development phase
25 participants
Enrollment target
3
Study locations

Study Summary

The purpose of the study is to find out the usefulness and safety of a dye called Indocyanine Green (ICG for short). This dye will be used to help the surgeon find lymph nodes draining solid tumors inside the abdomen that need to be removed. This may also help the surgeon to find if the cancer has moved to other lymph nodes outside of the known area. Primary Objectives * To determine the percentage of patients in whom Indocyanine Green (ICG)-guided sentinel lymph node (SLN) mapping was successful at the time of retroperitoneal lymph node dissection for staging of visceral solid tumors. * To determine the percentage of patients with grade 3 or higher adverse events related to ICG use.

Conditions Studied

Interventions

  • DRUG Indocyanine Green

Study Locations (3)

Illinois

  • Lurie Children's Hospital - Chicago

Pennsylvania

  • Children's Hospital of Pittsburgh of UPMC - Pittsburgh

Tennessee

  • St. Jude Children's Research Hospital - Memphis

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2023-10-24
Est. Completion 2026-12
Phase Early Phase 1

What the Registry Record Tells You About NCT05645523

The ClinicalTrials.gov registry entry for NCT05645523 describes a study currently listed as recruiting, categorized as Early Phase 1. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 222-participant average among 196 other Solid Tumor trials with a reported enrollment target (89% lower). The listed sponsor is St. Jude Children's Research Hospital, which has 410 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which Indocyanine Green is the first listed.

NCT05645523 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Illinois, Pennsylvania, Tennessee.

Frequently Asked Questions

What is clinical trial NCT05645523 about?

NCT05645523 is a clinical study titled "Indocyanine Green (ICG) Guided Sentinel Lymph Node Mapping for Pediatric Visceral Solid Tumors". The purpose of the study is to find out the usefulness and safety of a dye called Indocyanine Green (ICG for short). This dye will be used to help the surgeon find lymph nodes draining solid tumors inside the abdomen that need to be removed. This may also help the surgeon to find if the cancer has m...

What is the current status of trial NCT05645523?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 25 participants. The study started on 2023-10-24. Estimated completion is 2026-12.

What conditions does trial NCT05645523 study?

This clinical trial studies the following conditions: Solid Tumor.

What interventions are being tested in trial NCT05645523?

The interventions under investigation include: Indocyanine Green (DRUG).

Who is sponsoring clinical trial NCT05645523?

This trial is sponsored by St. Jude Children's Research Hospital, which has 410 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05645523 being conducted?

This trial has 3 study locations across Illinois, Pennsylvania, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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