Peri-Implantitis Clinical Trial
Official title:
Laser-Assisted Regenerative Surgical Therapy for Peri-implantitis: A Randomized Controlled Clinical Trial
The purpose of the study is to evaluate if using Erbium-doped yttrium aluminium garnet laser, Erbium YAG laser (Er:YAG) laser could have adjunctive benefits to the conventional standard mechanical debridement to ablate the infected tissue around the dental implant and detoxify the contaminated implant surface for resolving peri-implant infection and enhance bone regeneration of peri-implant defects.
The purpose of the study is to evaluate if using Er:YAG laser could have adjunctive benefits
to the conventional standard mechanical debridement to ablate the infected tissue around the
dental implant and detoxify the contaminated implant surface for resolving peri-implant
infection and enhance bone regeneration of peri-implant defects.
This study involves one center and a double-blinded randomized controlled clinical trial is
planned. Twenty-four adult patients in the need of surgical treatment due to peri-implantitis
will be included. Six visits are needed for each patient including a 24 week follow-up visit.
Specific Aim 1: To compare the clinical benefit of Er:YAG laser-assisted peri-implant defect
debridement and surface detoxification with conventional mechanical debridement for
regenerative therapy
Specific Aim 2: To evaluate whether Er:YAG laser-assisted regenerative surgical therapy can
decrease bacterial load and alter microbial profile
Specific Aim 3: To analyze whether Er:YAG laser-assisted regenerative surgical therapy can
impact the molecular profile of the peri-implant crevicular fluid (PICF) and the stability of
the treatment
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