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Gum treatment drugs under the microscope: are side effects being missed?

NCT ID NCT07666100

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study tracks 571 people receiving medications for gum disease in a periodontology clinic. Researchers will record any side effects, rate how severe they are, and check how they affect quality of life. The goal is to get a clearer picture of drug safety in everyday dental care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this study could help dentists better understand and manage medication side effects, improving patient safety and comfort during periodontal treatment.
What could go wrong
This is an observational study, not a treatment trial. It only collects data on side effects and does not test any new drug or therapy, so it won't directly change patient care.

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

About 571 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2026

Expected to finish

Sep 2027

An estimate. End dates often move.

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

Patients who receive treatment at the Department of Periodontology, Faculty of Dentistry, Sivas Cumhuriyet University between March 30, 2026 and September 30, 2027, who meet the inclusion criteria, and who have been prescribed any pharmacological agent will be included.

Ages

16 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: Being 16 years of age or older * Receiving treatment at a periodontology clinic • Having been prescribed at least one pharmacological agent * Volunteering to participate in the study and providing informed consent Exclusion Criteria: * Having a cognitive problem that would prevent the evaluation of side effects related to drug use * Patients who did not come for evaluation during the follow-up period or for whom sufficient follow-up data could not be obtained * Patients who provided incomplete, inconsistent or unreliable data regarding side effect evaluation

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As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Sivas Cumhuriyet University

    RECRUITING

    Sivas, Turkey (Türkiye)