The Effect of Dose and Storage Conditions of Indocyanine Green on Efficacy and Cost in Sentinel Lymph Node Mapping in Gynecological Cancer

NCT07380698 · tracked via the Priya Life Science Turkey tracker

Sponsor

Cukurova University

Phase

Observational

Started

2025-10-03

Last updated

2026-02-02

Condition(s) studied

Endometrial CancerVulvar CancersCervical CancerIndocyanine Green (ICG)

Study summary

This research will determine the impact of optimizing dosage and storage conditions for indocyanine green on health outcomes and will contribute to improving treatment processes in gynecological cancers. Ultrastaging will increase the detection of micrometastases. Furthermore, the cost impact of these optimizations will be evaluated. It will help develop more effective, safe, and cost-effective methods for sentinel lymph node mapping in gynecological cancers. Furthermore, significant savings in healthcare costs could be achieved.

Eligibility

Sex

FEMALE

Min age

—

Max age

—

Healthy volunteers

Inclusion Criteria: * cervical cancer, endometrial cancer, vulvar cancer, using indocyanine green, sentinel lymph node dissection Exclusion Criteria: \-

Primary outcome measure(s)

Sentinel lymph node detection success rate associated with optimized indocyanine green (ICG) dosage and storage conditions. — Baseline (pre-procedure), perioperative/periprocedural period, and up to 24 weeks post-procedure.

Trial sites (1)

Facility	City	Region	Status
Cukurova University	Adana	Turkey (Türkiye)	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07380698 on ClinicalTrials.gov ↗ ← All trials in Turkey