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The Role of Obesity in Peri-Implant Health(ROPIPH)

Evaluating the Influence of Obesity on Peri-Implant Health Through Clinical and Biochemical Parameters

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07183163
Acronym
ROPIPH
Enrollment
80
Registered
2025-09-19
Start date
2023-02-12
Completion date
2024-10-29
Last updated
2025-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Implant, Obesity &Amp; Overweight, Peri Implantitis

Keywords

obesity, peri-implant health, dental implants, peri-implant sulcus fluid, inflamatory iomarkers (IL-1B, TNF-a, MMP-8)

Brief summary

This clinical study aims to evaluate the influence of obesity on peri-implant health. Both clinical parameters and biochemical markers in peri-implant crevicular fluid(PICF) will be assessed. The study will include patients with dental implants who are classified as obese as well as a control group of non-obese participants. Clinical outcomes such as probing depth, plaque index, bleeding on probing, and peri-implant bone levels will be recorded. In addition, PICF samples will be analyzed for inflammatory biomarkers including interleukin-1 beta(IL-1beta), tumor necrosis factor-alpha(TNF-alfa), and matrix metalloproteinase-8(MMP-8). The results of this study may help to clarify the relationship between obesity and inflammatory responses in peri-implant tissues.

Detailed description

This prospective clinical study investigates the role of obesity in peri-implant health by assessing both clinical and biochemical parameters. The study population will consist of systemically healthy individuals aged 18 years or older who have undergone dental implant treatment. Participants will be categorized into obese and non-obese groups according to body mass index (BMI) and waist circumference measurements. Clinical evaluations will include plaque index, bleeding on probing, probing depth, and radiographic assessment of peri-implant marginal bone loss. PICF will be collected from implant sites using standardized paper strips. The collected fluid will be analyzed for inflammatory biomarkers, including IL-1 beta, TNF-alfa, and MMP-8 using enzyme-linked immunosorbent assay (ELISA). The primary objective of the study is to determine whether obesity is associated with altered peri-implant clinical parameters and increased levels of inflammatory biomarkers. By correlating clinical and biochemical findings with obesity-related measures (BMI and waist circumference), this study aims to provide valuable insights into the potential impact of obesity on peri-implant tissue health and the risk of peri-implant diseases.

Interventions

Assessment of peri-implant clinical parameters (probing depth, bleeding on probing, plaque index) and biochemical markers (IL-1β, TNF-α, MMP-8) in peri-implant crevicular fluid. No therapeutic or experimental intervention administered.

Sponsors

Mine Keskin
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults ≥18 years with dental implants in function for at least 1 year. * Patients diagnosed with peri-implantitis according to clinical and radiographic criteria. * For control group: systemically healthy individuals with peri-implant health. * Written informed consent obtained.

Exclusion criteria

* Patients with systemic diseases affecting periodontal/implant health (e.g., uncontrolled diabetes, HIV, cardiovascular disease, kidney disorders). * Pregnant or lactating women. * Current smokers or individuals using smokeless tobacco. * Alcohol abuse. * Use of antibiotics or anti-inflammatory drugs within the last 3 months. * Patients who had received peri-implant treatment within the last 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Levels of TNF-alfa in PICFBaselineTNF-alfa concentration in PICF will be quantified using ELISA. Samples will be collected from four sites per implant (mesial, distal, buccal, lingual). Higher levels indicate increased inflammation.
Levels of IL-1 beta in PICFBaselineIL-1beta concentration in PICF will be quantified using ELISA. Samples will be collected from four sites per implant (mesial, distal, buccal, lingual). Higher levels indicate increased inflammation.
Levels of MMP-8 in PICFBaselineMMP-8 concentration in PICF will be quantified using ELISA. Samples will be collected from four sites per implant (mesial, distal, buccal, lingual). Higher levels indicate increased inflammation.

Secondary

MeasureTime frameDescription
Probing depth around dental implantsBaselineProbing depth will be measured at six sites per implant using a periodontal probe. The mean value per implant will be recorded.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026