None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients visiting the hospital with peri-implant inflammation • A person who agrees to the study and is able to communicate • Adults over 20 and under 70 with good overall health • Those with mild to moderate inflammation and PPD exceeding 5 mm, bleeding or suppression upon probe, and loss of limbic bone exceeding 2 mm • A person who has agreed to periodontal therapy (gingival curattage) after local anesthesia for the area of inflammation around the implant • If there are multiple areas of inflammation around the implant in one person, select the worst area
Exclusion criteria
Exclusion criteria: • a person with an uncontrolled systemic disease • A person who has taken antibiotics within one month of visit 1 or is likely to take antibiotics during the study period; • Pregnant women or nursing women • People with acute symptoms around the prosthesis • A person who is sensitive to lactobacillus products including dairy products or has allergies (rhinitis, rash, diarrhea, abdominal pain, vomiting, itching, etc.) • A person who has consumed lactobacillus-containing food or health functional food within one week of the first visit;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bleeding on probing (BOP) | — |
Secondary
| Measure | Time frame |
|---|---|
| Gingival index (GI);Periodontal pocket depth (PD);Plaque inex (PI);oral microbiome | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital