Lasers in Peri-implantitis Treatment
NCT05733234 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2023-02-17
Summary
The current study aimed to investigate the effect of the combined Nd-Er: YAG laser on the surgical treatment of peri-implantitis by evaluating clinical markers and biomarkers of bone loss (RANKL/OPG). Twenty (20) patients having at least 1 implant diagnosed with peri-implantitis were randomly assigned to two groups for surgical treatment. In the test group (n=10), Er: YAG laser was used for granulation tissue removal and implant surface decontamination, while Nd: YAG laser was employed for deep tissue decontamination and biomodulation. In the control group (n=10), an access flap was applied, and mechanical instrumentation of the implant surface was performed by using titanium curettes. The following clinical parameters were evaluated at baseline and six months after treatment: Full-mouth Plaque Score (FMPS), Probing Pocket Depth (PPD), Probing Attachment Levels (PAL), recession (REC), and Bleeding on probing (BoP). Peri-implant crevicular fluid (PICF) was collected at baseline and six months for the evaluation of soluble RANKL and OPG utilizing enzyme-linked immunosorbent assay (ELISA).
Conditions
- Peri-Implantitis
Interventions
- DEVICE
-
Laser ,Fotona, Light Walker AT, Ljubljana, Slovenia
Laser is used adjunctively in the surgical treatment of peri-implantitis for decontamination of the implant surface
- DRUG
-
Mechanical Treatment
Dental instrument is used in combination with Chlorhexidine to decontaminate the implant surface
Sponsors & Collaborators
-
Aristotle University Of Thessaloniki
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-05-20
- Primary Completion
- 2022-03-21
- Completion
- 2022-03-21
- FDA Device
- Yes
Countries
- Greece
Study Locations
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