RecruitingNot ApplicableNCT06685523
Evaluation of Fractalkine and Its Receptor in Peri-implantitis
Evaluation of Fractalkine and Its Receptor in the Non-Surgical Treatment of Peri-implantitis
Sponsor
Kubilay BARIŞ
Enrollment
100 participants
Start Date
Nov 8, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
In this study, mechanical debridement group, Er:YAG laser group and diode laser group will be compared in terms of reducing peri-implant sulcus depth in the treatment of peri-implantitis.
Eligibility
Min Age: 40 YearsMax Age: 60 Years
Inclusion Criteria7
- Probing depth of 4-6 mm, bone loss of at least 2 mm on X-ray and presence of inflammatory symptoms in soft tissue
- No systemic disease that may affect the outcome of the treatment
- Patients with healthy periodontium or patients with completed periodontal treatment
- Individuals at least 6 months after prosthesis loading on the implant
- Individuals who do not require further surgery for the treatment of peri-implantitis
- Implants with at least 2 mm keratised gingiva
- Individuals aged 40-60 years
Exclusion Criteria5
- Individuals undergoing radiation therapy
- Individuals who smoke and drink alcohol
- Individuals in pregnancy or lactation
- Individuals who have received antibiotic treatment in the last three months
- Individuals with parafunctional habits
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Interventions
PROCEDURESubgingival debridement
To be applied 1 times (0. days)
PROCEDUREEr:YAG laser decontamination
To be applied 3 times
PROCEDUREDiyot laser decontamination
To be applied 3 times
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06685523
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