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NCT07054944Not yet recruiting

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)

Source: ClinicalTrials.gov · Last updated 26 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
10 (estimated)
First submitted
18 Jun 2025
Start date
Dec 2026
Primary completion date
Jul 2028
Lead sponsor
University of Rochester
NCT number
NCT07054944

What you commit to

  • Study type: Observational
  • Planned participants: 10
  • From Dec 2026 to the primary completion date, Jul 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with extensive prior surgery at the primary site or nodal basin expected to affect the lymphatic drainage.

Other illness

  • Subjects with a history of iodide allergies.

Other

  • Inability or unwillingness of research participant or parent/legal guardian to give written informed consent.
  • Currently pregnant.
  • Infants under 650 grams.

Who the study is looking for

  • 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.

Age in the registry: 1 month to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Rochester Medical Center
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.