NCT06479096

Four-Week Oral Malodor and Clinical Safety for a Concentrated Cosmetic Mouthwash

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 166 (actual)
• Sponsor: Johnson & Johnson Consumer and Personal Products Worldwide · Industry
• Sex: All
• Age: 18 Years – 99 Years
• Healthy volunteers: Accepted

Summary

The objective of this study is to evaluate the safety of the concentrated mouthwash prototypes, and to evaluate the efficacy of the concentrated mouthwash prototypes in the control of oral malodor compared to a comparator mouthwash and a negative control.

Conditions

• Oral Malodor

Interventions

Type	Name	Description
OTHER	Brush / Espresso Mild Prototype	Subjects will brush and rinse with their assigned mouthwash twice daily.
OTHER	Brush / Espresso Intense Prototype	Subjects will brush and rinse with their assigned mouthwash twice daily.
OTHER	Brush / Fresh Breath Oral Rinse	Subjects will brush and rinse with their assigned mouthwash twice daily.
OTHER	Brush / Hydroalcohol	Subjects will brush and rinse with their assigned mouthwash twice daily.

Timeline

• Start date: 2024-07-15
• Primary completion: 2024-09-12
• Completion: 2024-09-12
• First posted: 2024-06-27
• Last updated: 2025-01-08

Locations

1 site across 1 country: United States