Clin2
NCT07788001Possibly a fitNot yet recruiting

Comparing dye-guided lymph node removal versus standard method in esophageal cancer surgery

Esophageal CancerSentinel Lymph NodeLymphadenectomyIndocyanine Green (ICG)Disease Free Survival

Part of Cancer, Digestive system clinical trials.

This study compares two ways of finding and removing lymph nodes during esophageal cancer surgery. One uses a special dye (indocyanine green) to highlight lymph nodes, and the other is the standard method. The goal is to see if the dye method is as effective as the standard method while possibly being less invasive.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
200 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You are between 18 and 75 years old.
  • You have been diagnosed with esophageal squamous cell carcinoma or adenocarcinoma that has not spread to lymph nodes or distant organs.
  • You have not received any prior treatment for esophageal cancer (such as chemotherapy, radiation, or immunotherapy).
  • You are scheduled for minimally invasive removal of your esophagus and nearby lymph nodes.
  • You are in good health, with adequate heart, liver, and kidney function.
  • You have not had prior surgery on your esophagus or stomach.
  • You are not allergic to iodine or indocyanine green.
  • You do not have another cancer requiring treatment.
  • You are not pregnant or breastfeeding.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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