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PeriodontitisNCT07293481

Discovery and Validation of Periodontitis Biomarkers

An observational study of Periodontitis and Biomarker in Early Diagnosis, run by Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Periodontitis is a major public health issue in China: it is responsible for loss of masticatory function in 60 million older adults, and 400-500 million adults are on the same disease trajectory. In addition, gingivitis and early-stage periodontitis are highly prevalent in all age groups. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
What is being tested?
Diagnostic procedures
Type of treatment
Pill or oral medicine
How many people
228 participants
Where
1 siteChina
Study dates
21 Jul 2025to 31 Oct 2027
How long will I take part?
2 Years
Phase
Observational
Are there results?
Not yet: the study is under way

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 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: The study population consists of adult patients seeking care at Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, who are clinically diagnosed with gingivitis or stage I periodontitis. Participants are willing to contribute subgingival microbiome samples, oral fluid specimens, and optionally a small gingival tissue biopsy.

Who may be able to join

  • Adults between 18 and 40 years of age;
  • Diagnosed with varying degrees of periodontal disease, including gingivitis and stage I periodontitis;
  • Voluntarily agree to participate in the study, have signed the informed consent form, and are able to comply with the study protocol.

Who cannot join

  • Pregnant or breastfeeding women;
  • Individuals who have received antibiotic treatment within the past 3 months;
  • Individuals who have received periodontal treatment (including supragingival scaling) within the past 6 months;
  • Individuals with mucosal or salivary gland diseases (e.g., Sjögren's syndrome);
  • Individuals with severe systemic diseases, immune dysfunction, or health conditions that contraindicate surgery;
  • Individuals who are unwilling to cooperate with 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.

China1 site, 1 recruiting
  • Shanghai 9th people's hospital

    Shanghai, Shanghai Municipality, 200120

    Maurizio Tonetti, 86+15000102368, tonetti@shsmu.edu.cn

    Recruiting

Other trials in China

About this study

Periodontitis is a major public health issue in China: it is responsible for loss of masticatory function in 60 million older adults, and 400-500 million adults are on the same disease trajectory. In addition, gingivitis and early-stage periodontitis are highly prevalent in all age groups. The Lancet 2021 burden of disease study provides worrying projections for China's oral health, with a 47.8% increase in advanced-stage periodontitis and a 217% increase in edentulism by the year 2050. The numbers are not manageable by the Chinese health system unless a series of coordinated actions are implemented: i) health education promoting oral hygiene in school and the workplace; ii) effective AI-based self-detection strategies and accurate identification of high-risk subjects; iii) efficient treatment modalities; and iv) reorganization of the health system.

We have developed, patented, and validated a self-detection AI-based screening test for the general population through an app. It is based on a few validated questions and the performance of a lateral flow immunoassay to detect activated matrix metalloproteinase 8 (aMMP8). The algorithm enables accurate self-detection of severe periodontitis. The system, however, cannot identify subjects without clinically evident periodontitis (subjects who present with superficial inflammation consistent with gingivitis and incipient periodontitis) who will develop the disease, which, therefore, should be the target of early interventions. This limitation is due to insufficient knowledge of the process that turns superficial inflammation (gingivitis) into periodontitis. This limitation is apparent in the recently published NIH-sponsored American diagnostic trial results to detect periodontitis onset biomarkers (and progression). In their study, Teles et al. (2024) show that almost 24% of gingivitis subjects progress to periodontitis over a 12-month period but failed to identify salivary or serum biomarkers. Similarly, our recently completed study (Li et al. in preparation) did not identify highly accurate biomarkers for disease onset and progression. Importantly, the American and our study have tested putative biomarkers identified based on the current crude knowledge of the disease process. Gaps in fundamental knowledge are now apparent and limit our ability to detect periodontitis early. In addition, the current crude differential diagnosis based on clinical examination with a periodontal probe with millimeter markings cannot accurately differentiate gingivitis from early-stage periodontitis, complicating the ground truth definition (gold standard).

Read more

In the current study, we propose implementing a multi-omics approach to test the ability to discriminate a mixed population of clinically undifferentiable gingivitis and stage I periodontitis into two or more clusters. In this biomarker discovery phase, we plan to use multiple state-of-the-art methods: i) laser scanning microdissection proteomics of tissue biopsies, ii) conventional salivary proteomics, iii) tissue biopsy transcriptomics, and iv) shotgun microbiome analysis. The methods will be applied in an agnostic approach to test the following hypotheses:

  1. It is possible to identify two or more clusters of subjects from a mixed population of gingivitis and stage I periodontitis subjects.
  2. The clusters differ based on host-derived biomarkers and/or microbiome factors and the risk of progression to periodontitis.
  3. The biomarker pathways and microbial virulence factors among subjects identified according to the different approaches used to explore disease biology are generally consistent.
  4. It is possible to identify a limited set of biomarkers that can be used to predict periodontitis onset and thus target early interventions for this high-risk population.
Being tested
Diagnostic procedures
Medical subject headings
Periodontitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Diagnostic proceduresDiagnostic test

    All clinical measurements will be taken by a single trained and calibrated examiner using a PCP-UNC15 periodontal probe at a pressure of 0.25-0.3N.

    Unstimulated saliva, oral rinse, gingival crevicular fluid samples, subgingival microbiome samples, and gingival biopsies will be taken from the participants. All samples will be stored at -80C in standardized vials. Tissue samples will be divided into two equal portions: one will be fixed in paraffin for laser capture microdissection the other will be stored in liquid nitrogen for tissue transcriptomics. In addition, we will perform in depth microbiome analysis (shotgun approach and 16S) following the currently employed methods in use at our center.

Study groups in NCT07293481
Study groupRoleWhat they receive
A cohort of subjects with clinically undistinguishable gingivitis/stage I periodontitisNot described
Receives: Diagnostic Test: Diagnostic procedures

What is being measured

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

  1. Accuracy of biomarker-defined clusters in predicting periodontitis progression

    Biomarker-based clusters will be created using multi-omics data (proteomics, transcriptomics, microbiome). Their predictive accuracy for periodontitis progression will be assessed by comparing them to clinical outcomes after 24-month follow-up. Models will be optimized using AI-based feature selection techniques.

    Measured: 24 months

Timeline

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

  1. First posted19 Dec 2025
  2. Study start21 Jul 2025
  3. Primary completion31 Mar 2027 (estimated)
  4. Study completion31 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
Cohort
Time perspective
Prospective
Enrolment
228 participants (estimated)
Target duration
2 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07293481
Sponsor's protocol ID
SH9H-2024-T358-2
Status last verified
Apr 2026
First submitted
8 Dec 2025
Last updated
20 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Periodontitis and Biomarker in Early Diagnosis, run by Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Accuracy of biomarker-defined clusters in predicting periodontitis progression (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Apr 2026.

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