Condition: Postoperative Complications · Sponsor: Women and Infants Hospital of Rhode Island
The study will be a pilot randomized control trial with a 1:1 patient randomization of vancomycin powder placement at the time of surgery (compared to no vancomycin placement) with the goal of reducing postoperative complications in patients undergoing an inguinal lymph node dissection for vulvar cancer. The primary objective is to measure the composite rate of postoperative complications within 30 days of inguinal lymph node dissection in patients with vulvar cancer.
This description comes directly from the study's public registry record.
Jessica DiSilvestro, MD · 401-274-1100 · jdisilvestro@wihri.org
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| Women and Infants Hospital | Providence, Rhode Island, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05625373