Oral Health
Conditions
Interventions
Hexedene active
Oral Rinse Control
Sponsors
Department of Periodontics
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Participant must be between 18 and 60 years of age Participant must have ability to provide written informed consent, Participant must be in good general health as determined by the investigators, based on a review of the medical history Participant must have at least 20 gradable teeth, and Participant must have 10 or more bleeding sites at baseline
Exclusion criteria
Exclusion criteria: Known allergy or sensitivity to components of the oral rinse product, caries and restorations as well as dental appliance severe periodontal disease as characterized by purulent exudate, generalized mobility and/or severe recession, current active treatment for periodontal disease, bleeding disorder or use of a blood thinner, current orthodontic treatment, diabetes, pregnancy, antibiotic therapy within 3 months of the baseline visit any diseases or conditions that may interfere with the patient safely completing the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome will be improvement in plaque index and changes in gingival index, | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes will be changes in bleeding score, pocket depths, and changes in the composition of supragingival microbiome. | — |
Countries
Nigeria
Contacts
Public ContactJennifer Onagaumah
Senior Registrar
Outcome results
None listed