periodontitis
Conditions
Interventions
Intervention group (usual maintenance + periodontal disease treatment support application + measurement device) (Intervention period: 3 months after the start of the intervention) Periodontal mainten
Sponsors
Tokyo Medical and Dental University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 40 patients who visited Tokyo Medical and Dental University Hospital, completed periodontal disease treatment and were undergoing maintenance (no gender restriction)
Exclusion criteria
Exclusion criteria: Those with 19 or fewer remaining teeth Those whose molars have less than 4 units of occlusal support Removable Denture Users Persons with temporomandibular joint disorder Persons with verifiable oral motor impairment Persons with mental illness Currently receiving antimicrobial therapy Persons with serious systemic illnesses (who have been judged by a physician to be unacceptable for participation in this study)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plaque control record Preoperatively, 1 month, 3 months, and 6 months after the start of treatment (dummy in the control group), for a total of 3 times. | — |
Secondary
| Measure | Time frame |
|---|---|
| Probing Pocket Depth Bleeding On Probing Plaque Index Gingival Index Occult blood test Preoperatively, 1 month, 3 months, and 6 months after the start of treatment (dummy in the control group), for a total of 3 times. | — |
Countries
Japan
Contacts
Public ContactKoji Mizutani
Tokyo Medical and Dental University Department of Periodontology
Outcome results
None listed