Clinical Trials Directory

Trials / Completed

CompletedNCT02992314

Determination of the Safety and Effectiveness of an Oral Rinse in the Reduction of Medication Associated Metallic Taste

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
52 (actual)
Sponsor
You First Services · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Patients taking chemotherapeutic agents often do not comply well with their dosing regiment since many of these medications cause a metallic taste in the mouth. The primary intent is to determine the effectiveness of the oral rinse in reducing the metallic taste in the mouth associated with various chemotherapeutic agents. This clinical study a randomized, double-blind, single-treatment, parallel design with a placebo as the control. The duration of the trial will be 1 month.

Conditions

Interventions

TypeNameDescription
DEVICEMetaqil™ Oral RinseMetaqil™ is a proprietary formulation of GRAS ingradients
DEVICEPlaceboPlacebo formulation with out the active ingredients

Timeline

Start date
2017-05-22
Primary completion
2018-09-18
Completion
2018-12-31
First posted
2016-12-14
Last updated
2021-01-22

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT02992314. Inclusion in this directory is not an endorsement.