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A Study of Patients With Dry Mouth and Sticky Saliva During Radiotherapy

Xerostomia Clinical Trial

Official title:
Assessing the Safety and Effectiveness of Visco-ease for the Treatment of Radiotherapy Induced Xerostomia in Head and Neck Cancer Patients

Clinical Trial Summary

The purpose of this study is to evaluate the clinical safety and effectiveness of Visco-ease dry mouth spray for the treatment of Radiotherapy Induced Xerostomia (RIX) in head and neck cancer patients.

A parallel group double blind study design has been selected. The primary outcome is change in GRIX scores from baseline (visit 1) to end of treatment (visit 7). The primary outcome will be compared between Visco-ease and the placebo treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02687087
Study type Interventional
Source NHS Greater Glasgow and Clyde
Contact
Status Completed
Phase N/A
Start date March 24, 2016
Completion date February 2, 2017
View Details
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