LIHNCS: Lugol’s Iodine in Head and Neck Cancer Surgery
A multi-centre, randomised controlled trial assessing the effectiveness of Lugol’s Iodine to assist excision of moderate dysplasia, severe dysplasia and carcinoma insitu at mucosal resection margin of oral and oropharyngeal squamous cell carcinoma.
Principal Investigator: Jim McCaul
Trial Coordinator: Jacqueline Quantrill
Contact: Email not available without JavaScript
Tel: 01274 383921
Aim: This study is looking at whether the use of Lugol’s Iodine solution as a staining technique to detect dysplasia, helps reduce the incidence of dysplasia at resection margins in the surgical management of oral and oropharyngeal carcinoma and whether this in turn leads to a reduced risk of recurrence.
Funding: CRUK CTAAC
Opened: Oct 2010
Phase: Phase III
Recruitment Target: 300 by Nov 2013
Recruited 419 by Nov 2013
Milestones:
Funding confirmed Apr 2010
Ethics Approval Aug 2010
First site opened Oct 2010
First patient recruited Nov 2010
Ethics approval - Extension of trial from 300 patients to 419 patients – July 2013
Last site opened Aug 2013
Last patient recruited Nov 2013
Ethics approval extension of follow up to 5 years July 2015