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Recruiting NCT06520137

Third Molars Extraction and Periodontal Disease

— Observational Periodontal Diseases

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: Tooth extraction.
Who it may be relevant to
Registry conditions: Periodontal Diseases. Basic parameters: 19 years — 64 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
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Correlation Between Upper Third Molars Extraction and Upper Second Molars Periodontal Disease: a Prospective Clinical Observational Study

Overview

The aim of the study is to evaluate the changes in periodontal conditions on the distal aspect of the second maxillary molar after the extraction of the maxillary wisdom tooth. As secondary outcome patient- related and tooth-related factors will be analysed to evaluate their effects on the periodontal varibales during time.

Interventions

  • Procedure Tooth extraction
    Extraction of maxillary third molars

Primary outcome measures

  • Probing Pockeet Depth (PPD) [Time frame: Baseline, 1 month, 6 months, 12 months, 24 months]
  • Bone Level (BL) [Time frame: Baseline, 1 month, 6 months, 12 months, 24 months]
Secondary outcome measures (4)
  • Type of impaction [Time frame: Baseline]
  • Clinical Attachment Level (CAL) [Time frame: Baseline, 1 month, 6 months, 12 months, 24 months]
  • Recession (REC) [Time frame: Baseline, 1 month, 6 months, 12 months, 24 months]
  • Keratinized Tissue (KT) [Time frame: Baseline, 1 month, 6 months, 12 months, 24 months]

Eligibility criteria

Inclusion criteria

  • Age more than 18 years or older
  • Presence of an impacted upper wisdom tooth that need to undergo surgical extraction
  • Participants need to be able to sign and understand the informed consent and to follow the study-related procedures.

Exclusion criteria

  • People that have compromised general health conditions (ASA 3, 4, 5, 6)
  • Patients that assumed antibiotics in the last 6 months
  • Pregnant or breastfeeding women
  • Patients who suffer from periodontitis stage III and IV
  • Presence of a third molar with incomplete root formation is not taken into account for the surgical extraction.
  • Smoker patients

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • University of Siena — Siena

Identifiers

NCT: NCT06520137 · 26617

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗