Recruiting NCT06685523
Evaluation of Fractalkine and Its Receptor in Peri-implantitis
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Subgingival debridement, Er:YAG laser decontamination, Diyot laser decontamination.
- Who it may be relevant to
- Registry conditions: Peri-implantitis. Basic parameters: 40 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of Fractalkine and Its Receptor in the Non-Surgical Treatment of Peri-implantitis
Overview
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.
Interventions
- Procedure Subgingival debridement
To be applied 1 times (0. days) - Procedure Er:YAG laser decontamination
To be applied 3 times - Procedure Diyot laser decontamination
To be applied 3 times
Primary outcome measures
- Probing depth, clinical attachment loss [Time frame: sixth month]
Secondary outcome measures (1)
- gingival index, plaque index, sulcus blood index [Time frame: sixth month]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Turkey (Türkiye) · 1 center
- Kırıkkale University, Faculty of Dentistry, Department of Periodontology — Kirikkale
Identifiers
NCT: NCT06685523 · KU-DHF-KB-01