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Clinical Trial Summary

Primary objective

- To compare the incidence of postoperative nasal synerchia between Mitomicin C and placebo in patients at 6 months after endoscopic sinus surgery

- To validate the Thai version of disease-specific quality of life tool SNOT-22

Secondary objectives

- To compare the clinical signs and symptoms of CRS in patients who receive Mitomicin C with those who receive placebo

- To compare the disease-specific quality of life in patients who receive Mitomicin C with those who receive placebo

- To compare the side effects of Mitomicin C versus placebo


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02106793
Study type Interventional
Source Mahidol University
Contact
Status Completed
Phase Phase 3
Start date March 2015
Completion date December 1, 2017

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