drugset / Trial / NCT06251089

Effect of Cetylpyridinium Chloride (CPC) Rinse in Viral Upper Respiratory Tract Infections (vURTI)

NCT06251089

Completed 102 enrolled Dentaid SL Methodex · collab
RandomizedParallel-groupDouble-blindPrevention

Summary

This is a randomized, controlled clinical trial with two parallel groups in which 150 volunteers (75 per group) will receive either VITIS CPC Protect® mouthwash (Mouthwash with cetylpyridinium chloride (CPC) as an anti-plaque antiseptic at a concentration of 0.07%) or mouthwash without cetylpyridinium chloride, as control group Subjects included in the study will be followed for 90 days. Symptoms associated with vURTIs (viral upper respiratory tract infections) should be recorded, when they appear, to determine the existence of viral infections of the upper respiratory tract. Symptoms and adverse effects will be recorded when the episode occurs. The assignment as VURIs will be made by the investigator once the diaries have been completed, or during the symptoms if possible.

Timeline

Start
2023-11-15
Primary completion
2024-08-05
Completion
2024-08-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetylpyridinium Small molecule 0.07 % Oral

Indications