Peri-Implantitis
Conditions
Keywords
Laser
Brief summary
The present study represents an extension of the previously concluded randomized clinical trial Laser-Assisted Regenerative Surgical Therapy for Peri-implantitis (HUM00124386). The aim of the study is to compare the adjunctive effect of laser over mechanical debridement alone in the maintenance of peri-implant tissues after surgical treatment of peri-implantitis (gum disease around implants).
Detailed description
The same 24 subjects, previously treated with surgical regenerative treatment of peri-implantitis following the LARST protocol, will be invited to return for three follow-up visits. During the follow-up visits, clinical measurements, x-rays, and pictures of the inside of their mouth will be taken to evaluate the success of their peri-implantitis treatment. If needed, additional laser treatment of the dental implant may also be provided according to the same randomization of subjects in the original study. No placebo laser application will be provided.
Interventions
Soft tissue implant measurements and radiographs
Sponsors
Study design
Eligibility
Inclusion criteria
* Subjects who were previously enrolled subjects in the randomized clinical trial of laser-assisted regenerative surgical therapy
Exclusion criteria
* Unable to reach the subject * The implant is mobile or lost Premature
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Periodontal Probing Depths (PD) | Baseline and 6 months | PD will be measured in millimeters. Change in PD measurements were calculated between baseline and 24 weeks |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Clinical Attachment Level (CAL) | Baseline and 6 months | CAL will be measured in millimeters. Change in subject CAL measurements were calculated between baseline and 6 months. |
| Change in marginal bone level (MBL) | Baseline and 6 months | Marginal bone level will be measured compared to baseline. Participants' standardized radiographs will be used to determine bone level changes between baseline and 6 months. |
Countries
United States