NCT06685523RecruitingNot Applicable
Evaluation of Fractalkine and Its Receptor in the Non-Surgical Treatment of Peri-implantitis
Kubilay BARIŞ1 site in 1 country100 target enrollmentStarted: November 8, 2024Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Probing depth, clinical attachment loss
Study Overview
Brief 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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 40 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •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 Criteria
- •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
Arms & Interventions
Mechanical debridement group
Experimental
Intervention: Subgingival debridement (Procedure)
Er:YAG laser applied group
Experimental
Intervention: Er:YAG laser decontamination (Procedure)
Diyot laser applied group
Experimental
Intervention: Diyot laser decontamination (Procedure)
Group healty
No Intervention
Outcomes
Primary Outcomes
Probing depth, clinical attachment loss
Time Frame: sixth month
Measurement will be made with a periodontal probe. The unit of measurement is millimetre. The primary outcome measures are interrelated.
Secondary Outcomes
- gingival index, plaque index, sulcus blood index(sixth month)
Investigators
Kubilay BARIŞ
Assistant Professor
Kırıkkale University
Study Sites (1)
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