Clinical Study to Assess Therapeutic Delay and Resolution of Induced Gingivitis

Conditions: Gingivitis

Sex: All

Ages: 18 Years – 70 Years

Healthy volunteers: 1

Phase: PHASE4

Enrollment: 26

Sponsor: Colgate Palmolive

Location: Canada

Summary

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

Eligibility Criteria

Inclusion Criteria:Male or female volunteers aged 18-70 yearsIn good general health, ASA INo clinical signs of gingival inflammation at >90% sites observedProbing Depth (PD) < 3.0 mmAttachment Loss (AL) = 0 mmNo periodontal disease historyNon-smokersFluent in EnglishExclusion Criteria:Presence of orthodontic bands.Presence of partial removal dentures.Tumour(s) of the soft or the hard tissues of the oral cavity.Cavitated carious lesions requiring immediate restorative treatment.History of allergy to consumer or personal care products or dentifrice ingredients as determined by the dental profession monitoring the study.Participation in any other clinical study or test panel with a one month period prior to entering the study.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05731778). StuddyBuddy aggregates publicly available trial information.