peri implantitis. Post-osseointegration biological failure of dental implant
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 18-80 years of age Presence of at least one site with peri-implantitis (PPD= 6mm, MBL=3 mm and bleeding/suppuration on probing) At least 1 year of function in implants Screw type implants with rough surface
Exclusion criteria
Exclusion criteria: Use of antibacterial or non-steroidal anti-inflammatory drugs within 3 months prior to diagnosis Implant mobility Pregnancy or breastfeeding History of autoimmune diseases, malignancy, cardiovascular insufficiency or acute diseases of other organs History of peri-implantitis or periodontal treatment in last 6 months Uncontrolled diabetes (HbA1c > 7%) Tobacco use
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Probing pocket depth(PPD). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: plastic probe.;Clinical attachment loss(CAL). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: plastic probe.;Papillary bleeding index(PBI). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: Observation of papillary bleeding pattern.;Modified mombelli plaque index(mPI). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: Observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Islamic Azad University