CelAgace™ OraRinse Solution for Treatment of Candidiasis

Status Not yet recruiting

Clinical Trial Summary

CelAgace™ OraRinse (silver citrate complex and acemannan) Solution is planned to be evaluated for safety and effectiveness as a potential treatment for candidiasis, a yeast infection, commonly known as thrush, which is associated with mouth sores.

Clinical Trial Description

CelAgace™ contains two active ingredients, a silver citrate complex salt (0.01mg/ml) that has demonstrated laboratory effectiveness against yeast organisms and acemannan (4.0mg/ml), a purified extract isolated from the inner leaf gel of the Aloe vera plant that has been used as a key ingredient in other oral care products. Patients will swish and spit the product 4 times daily (after meals and at bedtime) for 14 days. Following an initial office visit, patients will be evaluated on days 7 and 14 to determine response to the product. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03250923
Study type	Interventional
Source	CelaCare Technologies, Inc.
Contact	Jacqueline M. Plemons, DDS, MS
Phone	214-828-8467
Email	jplemons@tamhsc.edu
Status	Not yet recruiting
Phase	Phase 1/Phase 2
Start date	September 2024
Completion date	May 2025

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