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Spots Global Cancer Trial Database for Sentinel Lymph Node Procedure in Testicular Germ Cell Tumour

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Trial Identification

Brief Title: Sentinel Lymph Node Procedure in Testicular Germ Cell Tumour

Official Title: Sentinel Lymph Node Procedure in Testicular Germ Cell Tumour

Study ID: NCT03448822

Study Description

Brief Summary: Assessment of accuracy of sentinel node biopsy, defined as the false negative rate.

Detailed Description: Current practice in patients with Clinical Stage I (CS I) testicular germ cell tumour is active surveillance after orchiectomy, with relapses occurring in 15-20% of patients. The majority of relapses occur in the lymph nodes as lymphogenic spread is the dominant route of dissemination. A sentinel node procedure, in which the sentinel lymph node is resected and pathologically examined, could be more reliable to identify patients who are likely to relapse. Early identification of patients with micro-metastases in the sentinel node makes it possible to treat these patients at the earliest possible moment. Absence of metastases could lead in the future to a less intensive follow up protocol than the present one.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Contact Details

Name: Simon Horenblas, MD, PhD

Affiliation: NKI-AvL

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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