AI predicts best gum treatment for each patient

NCT ID NCT07485946

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 08, 2026 · Updated 2 times

Summary

This study aimed to create a computer model that can predict which gum disease treatment will work best for each person. Researchers looked at dental records from 86 patients, including gum measurements, X-rays, and personal details. The goal is to help dentists choose the most effective treatment plan for each individual.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

126 people

The number who actually took part.

Started

Aug 2025

Finished

Jan 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consists of patients diagnosed with periodontitis who attended the Department of Periodontology, Faculty of Dentistry, Akdeniz University, between 2021 and 2025. Patients were identified retrospectively from archived clinical and radiographic records. Eligible patients had completed active periodontal therapy and had complete baseline and follow-up records. The analytical unit was the tooth; only periodontally involved teeth with documented treatment modality and measurable treatment outcomes were included in the predictive analyses.

Ages

16 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Patients with a confirmed diagnosis of periodontitis according to the 2017 AAP/EFP classification, supported by complete clinical and radiographic records. 2. Availability of baseline clinical periodontal examination and radiographic records before periodontal treatment. 3. Completion of active periodontal therapy, including non-surgical periodontal treatment and/or surgical periodontal treatment when clinically indicated. 4. Availability of at least one post-treatment follow-up visit after completion of active periodontal therapy. 5. Presence of at least one periodontally involved tooth meeting tooth-level eligibility criteria. 6. Availability of detailed tooth-level documentation, including baseline periodontal measurements, radiographic assessment, documented treatment modality, and corresponding post-treatment outcome records. 7. Teeth were eligible for tooth-level analysis if they received one of the predefined periodontal treatment modalities: non-surgical periodontal treatment, conventional flap surgery, or regenerative periodontal surgery. 8. Patients with a previous history of cancer were eligible if chemotherapy or radiotherapy had been completed and medical clearance for periodontal treatment had been obtained. Exclusion Criteria: 1. Incomplete demographic, clinical, radiographic, treatment, or follow-up records. 2. Unclear or undocumented periodontal treatment modality. 3. Systemic conditions contraindicating periodontal treatment or substantially affecting periodontal treatment outcomes. 4. Pregnancy or breastfeeding at the time of periodontal treatment. 5. Ongoing chemotherapy or radiotherapy. 6. Current or previous bisphosphonate therapy affecting periodontal or surgical treatment eligibility. 7. Presence of an immunocompromised condition. 8. Acute systemic illness or active infection at the time of periodontal evaluation or treatment. 9. Teeth with missing baseline or follow-up periodontal measurements, missing radiographic assessment, unclear treatment allocation, or insufficient documentation for outcome assessment were excluded from the tooth-level analysis.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Akdeniz University

    Antalya, konyaaltı, 07070, Turkey (Türkiye)

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