peri-implantitis. Other endosseous dental implant failure
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Presence of pre-implant disease No history of pre-implant surgery treatment PD>6 mm Positive BOP BOL<2mm No use of antibiotics and mouthwash and periodontal treatment in the last 6 weeks. No use of antibiotics and mouthwash and periodontal treatment in the last 6 weeks
Exclusion criteria
Exclusion criteria: Pregnancy and breast feeding Using anticoagulants Allergy to tetracycline sterile eye ointment Underlying disease (diabetes, kidney disorders, etc.) Smoking
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Presence or absence of plaque on tooth and implant surfaces (mesial, distal, buccal and lingual surfaces). Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.;The distance between the gingival margin and the depth of the envelope is in millimeters. Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.;Presence or absence of bleeding after probing. Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination.;The distance between the acrylic stent and the depth of the pocket. Timepoint: 1 and 3 months after the intervention. Method of measurement: Clinical dental examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences