None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The study group comprised of 24 systemically and periodontally healthy patients above 18 years of age of both the sexes. Periodontal health defined as no probing attachment loss, less than or equals to 3 mm probing pocket depth, less than 10 percent bleeding on probing.
Exclusion criteria
Exclusion criteria: Presence of systemic disease, requirement of endocarditis prophylaxis before dental treatment, untreated caries, gingival hyperplasia or other severe oral diseases, presence of orthodontic appliances or removable dentures, antibiotic therapy less than 3 months and mouthrinse use less than 8 weeks prior to baseline examination, manifestation of xerostomia, smoking habit, hypersensitivity or allergy to Chlorhexidine gluconate and Octenidine dihydrochloride., pregnancy and lactation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To quantitatively assess the effect of OCT on plaque growth on plaque free surfaces when used as an exclusive plaque control measure.Timepoint: 45 days | — |
Secondary
| Measure | Time frame |
|---|---|
| To comparatively evaluate the amount of plaque reformation after the use of Octenidine dihydrochloride (OCT), Chlorhexidine gluconate (CHX) and Mechanical plaque control. To comparatively assess the level of gingival inflammation after the usage of OCT, CHX and Mechanical plaque control.Timepoint: 45 days | — |
Countries
India
Contacts
Sudha Rustagi college of dental sciences and research