Clinical Study to Assess Therapeutic Delay and Resolution of Induced Gingivitis

• Status: Completed
• Trial end date: 2020-12-22
• Target enrollment: 0
• Participant gender: All

Summary

Evaluate a stannous technology for its effect on the neutrophil phenotype during an induced gingivitis state.

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Colgate Palmolive
• Treatments: Fluorides; Listerine; Sodium Fluoride; Tin Fluorides

Criteria

Inclusion Criteria:

1. Male or female volunteers aged 18-70 years

2. In good general health, ASA I

3. No clinical signs of gingival inflammation at >90% sites observed

4. Probing Depth (PD) < 3.0 mm

5. Attachment Loss (AL) = 0 mm

6. No periodontal disease history

7. Non-smokers

8. Fluent in English

Exclusion Criteria:

1. Presence of orthodontic bands.

2. Presence of partial removal dentures.

3. Tumour(s) of the soft or the hard tissues of the oral cavity.

4. Cavitated carious lesions requiring immediate restorative treatment.

5. History of allergy to consumer or personal care products or dentifrice ingredients as determined by the dental profession monitoring the study.

6. Participation in any other clinical study or test panel with a one month period prior to entering the study.