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Contrast-enhanced Ultrasound for Sentinel Node Detection
Sponsor: The Netherlands Cancer Institute
Summary
This is a prospective single-center interventional non-inferiority study where subjects are participating for one day for patients 18 years or older with melanoma, breast cancer or head \& neck cancer (including melanoma of head and neck area) and scheduled for a surgical SN procedure in the NKI-AvL without any contra-indication for Sonazoid contrast agent, such as an allergy to eggs or egg products. The primary objective is to assess the sensitivity of CEUS for intra-operative SN localization compared to the gold standard (99mTc nanocolloid). Secondary objectives are the specificity of CEUS for intra-operative SN localization, the time required to localize the SNs using CEUS and intraoperative usability of the CEUS-system. The primary endpoint is the sensitivity of the CEUS SN localization method. The conventional gamma probe will be used as ground truth comparison.
Official title: Contrast-enhanced Ultrasound for Sentinel Node Detection in Patients With Melanoma, Breast Cancer or Head & Neck Cancer
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
91
Start Date
2025-09-18
Completion Date
2026-09-18
Last Updated
2025-12-30
Healthy Volunteers
No
Conditions
Interventions
Sonazoid
Intradermal injection of the ultrasound contrast agent Sonazoid.
Locations (1)
Netherlands Cancer Institute
Amsterdam, North Holland, Netherlands