RecruitingNCT07054944

Tumor-Lymph Node Mapping

FEASIBILITY AND SAFETY OF INDOCYANINE GREEN (ICG) GUIDED SENTINEL LYMPH NODE MAPPING FOR PEDIATRIC SOLID TUMORS - T-LyM (Tumor-Lymph Node Mapping)


Sponsor

University of Rochester

Enrollment

10 participants

Start Date

Apr 13, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to assess the feasibility and safety of ICG-guided intraoperative lymphography for detecting sentinel lymph nodes (SLN) in pediatric patients with solid tumors who require retroperitoneal lymph node dissection/sampling. This trial is a single-site cross-sectional study. The injection of ICG directly into lymphatics draining the primary tumor will take place at the time of operation after the patient is under anesthesia.


Eligibility

Min Age: 1 MonthMax Age: 17 Years

Inclusion Criteria3

  • Any pediatric patient (under the age of 18 years) being treated at the University of Rochester Medical Center, Department of Surgery.
  • Diagnosed with pediatric solid tumor
  • Scheduled to undergo lymph node sampling as part of their clinical management.

Exclusion Criteria5

  • Subjects with a history of iodide allergies.
  • Inability or unwillingness of research participant or parent/legal guardian to give written informed consent.
  • Currently pregnant.
  • Infants under 650 grams.
  • Patients with extensive prior surgery at the primary site or nodal basin expected to affect the lymphatic drainage.

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Interventions

DIAGNOSTIC_TESTICG (Indocyanine Green)

Lymphatic mapping


Locations(1)

University of Rochester Medical Center

Rochester, New York, United States

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NCT07054944


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