Efficacy of regenerative surgical therapy using Er: YAG laser for peri-implantitis: a randomized controlled clinical trial
Not Applicable
- Conditions
- Peri-implantitis
- Registration Number
- JPRN-UMIN000026229
- Lead Sponsor
- iigata University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
Not provided
Exclusion Criteria
1.Persons who had received non-surgical peri-implant therapy within the previous 3 months 2.Persons who had received surgical peri-implant therapy within the previous 6 months 3.Persons who had taken systemic antibiotics or anti-inflammatory drugs within 3 months before experiment 4.Acute periodontal burden on the study implant and the adjacent natural tooth 5.Smoker 6.Persons who had severe systemic diseases 7.Persons who are pregnant or suspected to be pregnant 8.Pacemaker or any other systemic conditions that might be affected by the Er: YAG laser treatment 9.Persons who are judged to be unqualified for this study subjects by investigators.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method