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Recruiting Observational

Transcriptome, Proteome and Microbiome Profile in Periodontal and Peri-implant Diseases

NCT06262035 · tracked via the Priya Life Science Sweden tracker
Phase
Observational
Started
2024-06-15
Last updated
2024-10-10

Condition(s) studied

Peri-implantitisPeriodontitis

Investigational drug(s) / intervention(s)

Periodontitis and Peri-implantitis

Periodontitis and Peri-implantitis: Defined periodontitis at ≤ 2 non-adjacent teeth AND Defined peri-implantitis at ≤ 1 implant, in function of at least 1 year.

Study summary

1. To investigate the transcriptomic profile of periodontitis and peri-implantitis. Patients with defined periodontitis, at two non-adjacent teeth and peri-implantitis at ≥ one implant in function of ≥ one year, will be included to investigate the gene expression profile in tissue affected by periodontitis and peri-implantitis. Subjects will undergo a full-mouth examination performed by a calibrated examiner, including assessment of caries, bone abnormalities and infections according to intraoral x-ray, plaque index and pocket probing depth, suppuration, bleeding on probing, alveolar bone loss, and the number of teeth. During surgical intervention, tissue biopsies (two specimens per site) will be collected by a periodontist from site with ongoing periodontitis and site from ongoing peri-implantitis.
2. To study the microbiome and biomarker profile associated with periodontitis and peri- implantitis. Patients with defined periodontitis, at two non-adjacent teeth and peri-implantitis at ≥ one implant in function of ≥ one year, will be included in this study to determine the bacteria composition, cytokine profile and inflammatory biomarkers profile. Subjects will undergo a full-mouth examination performed by a calibrated examiner, including assessment of caries, bone abnormalities and infections according to intraoral x-ray, plaque index and pocket probing depth, suppuration, bleeding on probing, alveolar bone loss, and number of teeth. Peri-implant crevicular fluid (PICF), gingival crevicular fluid (GCF), saliva and submucosal/subgingival plaque will be collected.The presence and composition of periodontal and peri-implant plaque samples are investigated.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: ≥18 years of age Defined periodontitis at two non-adjacent teeth Defined peri-implantitis at ≥1 implant Signed informed consent Exclusion Criteria: Surgical intervention of periodontitis and/or peri-implantitis during last 6 months. Local or systemic use of antibiotics during last 6 months.

Primary outcome measure(s)

  • Protein levels in peri-implantitis and periodontitis — Through study completion, an average of 1 years
    To measure protein levels in gingival crevicular fluid and in peri-implant crevicular fluid.
  • Microbiome composition in peri-implantitis and periodontitis using 16S-rRNA sequencing method. — Through study completion, an average of 1 years
    The microbiome composition will be analyzed in samples of subgingival/submucosal plaque using 16S-rRNA sequencing method.
  • Gene expression profile in peri-implantitis and periodontitis. — Through study completion, an average of 1 years
    Soft tissue specimens will be studied in regards of gene expression levels using RNA sequencing method (Ilumina). The mRNA expression of candidate genes will be studied at protein level using immunohistochemistry.

Trial sites (1)

FacilityCityRegionStatus
Aqua Dental Specialistklinik Stockholm Sweden Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06262035 on ClinicalTrials.gov ↗ ← All trials in Sweden