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Clinical Trial Summary

Evaluation of removal of Sentinel lymph nodes only for detection of pelvic lymph node metastases in high risk and low risk endometrial cancer.


Clinical Trial Description

Consecutive patients with- and low risk endometrial cancer will be approached for eligibility for inclusion in a study evaluating the detection rates of pelvic metastatic disease by detection and removal of Sentinel lymph nodes only, i.e with no further lymphadenectomy.

A re-staging will be performed in case of metastatic Sentinel lymph nodes to guide adjuvant treatment.

The detection rate will be evaluated from a non-inferiority perspective against the expected rate of nodal metastases based on detailed final histological data.

Adverse events related the intervention ( Injection of tracer (ICG) and removal of sentinel nodes), time for the intervention, and an objective evaluation of lymphatic complications (lymphoedema) will be performed in addition to the use of a validated lymphoedema QOL questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03838055
Study type Interventional
Source Region Skane
Contact Jan Persson, Ass prof
Phone 0046733522080
Email jan.persson@med.lu.se
Status Not yet recruiting
Phase N/A
Start date February 2019
Completion date December 2023

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