Optimizing indocyanine green dose and storage for sentinel lymph node mapping in gynecologic cancers

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will follow patients with endometrial, cervical, or vulvar cancer who undergo sentinel lymph node (SLN) mapping using indocyanine green (ICG) to compare different ICG doses and storage conditions. Investigators will record SLN detection rates, bilateral mapping success, and ultrastaging results to capture micrometastasis detection. The study will also collect cost and supply data to model potential savings from optimized dosing and storage practices. All participants receive standard surgical care at the study site while additional data are collected non‑interventionally.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* cervical cancer, endometrial cancer, vulvar cancer, using indocyanine green, sentinel lymph node dissection

Exclusion Criteria:

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Where it's running

• Cukurova University
  Adana, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: Ghanim Khatib, MD
• Email: ghanim.khatib@gmail.com
• Phone: +903223386060

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.