periimplantitis. Presence of tooth-root and mandibular implants, Gingivitis and periodontal diseases
Conditions
Interventions
Intervention 1: Control group: They will only be treated with mechanical debridement and Laser radiation will also be symbolically displayed in this group without turning on the device. Intervention 2
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 Patients in good systemic health Having at least 1Implant that is been loaded for more than 1 year and has more than 1/5 mm Marginal Bone Loss(MBL) from the attachment level of Abutment and Fixture
Exclusion criteria
Exclusion criteria: Smoking or drinking alcohol Pregnancy or breastfeeding Using Antimicrobial or Antiinflamatory Medication over past 2 months History of Periodontal surgery in past year
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Probing depth: the pocket depth from the mucosa margin to the bottom of the peri-implant sulcus. Timepoint: before treatment , after 6 weeks and 6 months after the intervention. Method of measurement: physical examination.;Bleeding on probing: The presence or absence of bleeding from gingival sulcus15 seconds after implantation around the implant. Timepoint: before treatment , after 6 weeks and 6 months after the intervention. Method of measurement: physical examination.;Marginal bone loss: Bone margin Distance from Fixture Abutment Connection. Timepoint: before treatment , after 6 weeks and 6 months after the intervention. Method of measurement: radiographic examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactYasaman Sanaei
Ahvaz University of Medical Sciences
Outcome results
None listed