Multicenter Selective Lymphadenectomy Trial II (MSLT-II)

Clinical Trial Summary

Subjects must be diagnosed with melanoma. All subjects receive sentinel lymphadenectomy. If the subject is sentinel node positive and meets study requirements, the subject is randomized to receive either (1) completion lymphadenectomy (2) observation with nodal ultrasound. Subjects are then followed for 10 years.

See also
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NCT number	NCT00297895
Study type	Interventional
Source	Saint John's Cancer Institute
Contact
Status	Completed
Phase	N/A
Start date	September 30, 2004
Completion date	September 30, 2019

Multicenter Selective Lymphadenectomy Trial II (MSLT-II)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms