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Clinical Evaluation of MucoPEG™ for Xerostomia — CEMPEG  

Xerostomia Clinical Trial

Official title:
Clinical Evaluation of MucoPEG™ for Xerostomia

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of the oral rinse comparing to MucoPEG™ and Biotene®. This is a randomized open-label crossover study with 42 patients receiving treatment. Patients will be randomly assigned to receive either the MucoPEG™ or the Biotene® Dry Mouth Gentle Oral Rinse in the first period. Patients will use the assigned oral rinse two times a day for two weeks. Patients will switch to the other treatment after a wash-out period of one week.

Clinical Trial Description

The purpose of this study is to compare MucoPEG™ and it temporal change to those of the Biotene® Dry Mouth Gentle Oral Rinse in patients with Xerostomia. The study will gather data on patient reported outcomes on the safety and performance of the product, mouth-feel qualities and any changes in dry mouth. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04986501
Study type Interventional
Source SunBio, Inc.
Contact
Status Completed
Phase N/A
Start date May 2, 2022
Completion date November 15, 2022
View Details
See also
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