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Periodontitis, AdultPAROCHEWNCT07665489

Evaluation of Masticatory Performance in Patients With Periodontitis

An observational study of Periodontitis, Adult and Periodontitis, run by University Hospital, Clermont-Ferrand at 1 site in France.

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Sites and contacts
Official record

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Trial summary

The objective of this observational study is to assess the correlation between the severity of periodontal involvement and masticatory performance in patients with periodontitis. The secondary objectives are to identify periodontal parameters that may be associated with a reduction in masticatory performance. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Periodontitis, Adult, Periodontitis, Oral Disease
How many people
100 participants
Where
1 siteFrance
Study dates
9 Oct 2026to 9 Oct 2027
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients diagnosed with periodontitis and followed at a university hospital (CHU), recruited during routine periodontal care.

Who may be able to join

  • Patients followed at the university hospital (CHU) with a diagnosis of periodontitis.
  • No objection from the patient to participate in the study.
  • Patients able to speak and understand French.

Who cannot join

  • Minors.
  • Patients under legal protection (guardianship, trusteeship, or judicial protection measures).
  • Pregnant or breastfeeding women.
  • Patients who refuse to participate in the study.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • CHU Clermont-Ferrand

    Clermont-Ferrand

    Lise Laclautre, 0473754963, promo_interne_drci@chu-clermontferrand.fr

    Thomas DOUILLARD

    Recruiting

Other trials in France

About this study

The objective of this observational study is to assess the correlation between the severity of periodontal involvement and masticatory performance in patients with periodontitis.

The secondary objectives are to identify periodontal parameters that may be associated with a reduction in masticatory performance.

This study includes a single group.

Participants will be asked to perform a masticatory performance test consisting of chewing a piece of gum for 20 cycles.

Read the detailed description

The study will be conducted over a one-year period. Patients diagnosed with periodontitis during their treatment within the Department of Dentistry will be invited to participate in the study. After being provided with clear information about the study and after their lack of objection has been recorded, they will be asked to undergo a masticatory performance test consisting of chewing a piece of chewing gum. The chewing gum samples collected at the end of this test will be analyzed in the CROC laboratory to determine a masticatory performance value. All collected data will then be analyzed to address the study objectives.

Medical subject headings
Chronic Periodontitis, Periodontitis, Mouth Diseases

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Value of the patient's masticatory performance

    Value of the patient's masticatory performance, obtained from the masticatory performance test (two-color chewing gum test) (quantitative variable).

    Measured: Baseline

Secondary outcomes (7)
  1. Severity of periodontal disease assessed by stage.

    Stage of periodontitis according to the Chicago classification. Categorical (Stage 1 (early-stage periodontitis) to Stage 4 (severe periodontitis) as defined by classification)

    Measured: Baseline (T0)

  2. Pocket Depth

    Periodontal probing depth. Unit of Measure: Millimeters (mm)

    Measured: Baseline

  3. Gingival recessions

    Measurement of gingival recession depth. Unit of Measure : Millimeters (mm)

    Measured: Baseline

  4. Bleeding on Probing (BOP)

    Percentage (%) of sites showing bleeding on probing.

    Measured: Baseline

  5. Plaque Index

    Plaque accumulation assessed using a validated plaque index (specify full name of index).

    Measured: Baseline

  6. Tooth Mobility

    Tooth mobility assessed using the Miller classification (Grade 0-3). Higher scores indicate greater mobility and worse periodontal condition. Unit of Measure: Millimeters (mm)

    Measured: Baseline

  7. Edentulism

    Presence or absence of edentulism.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2026
  2. Study start9 Oct 2026
  3. Primary completion9 Oct 2027 (estimated)
  4. Study completion9 Oct 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07665489
Sponsor's protocol ID
RNI 2026 DOUILLARD
Acronym
PAROCHEW
Status last verified
Oct 2026
First submitted
11 Jun 2026
Last updated
16 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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