Actively Recruiting
Evaluation of Fractalkine and Its Receptor in Peri-implantitis
Led by Kubilay BARIŞ · Updated on 2024-11-12
100
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Evaluation of Fractalkine and Its Receptor in Peri-implantitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kırıkkale University, Faculty of Dentistry, Department of Periodontology
Kirikkale, Turkey (Türkiye), 71000
Actively Recruiting
Research Team
K
Kubilay Barış, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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