Could popular Weight-Loss drugs harm your teeth? a new study investigates
NCT ID NCT07720466
First seen Jul 22, 2026 · Last updated Jul 23, 2026 · Updated 1 time
Summary
This study looks at whether GLP-1 receptor agonists like semaglutide and tirzepatide, used for weight loss, change saliva composition and increase tooth wear. Researchers will measure saliva calcium, pH, flow rate, and dental erosion in 40 adults before and 3 months after starting the medication. The goal is to understand potential oral health side effects and help clinicians prevent dental complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- semaglutide or tirzepatide (GLP-1 receptor agonists)
- What this could lead to
- If it finds clear links, this could help doctors monitor and prevent dental problems in people taking GLP-1 drugs for obesity.
- What could go wrong
- This is a small, early observational study with only 40 participants and no control group, so results may not apply broadly. It measures changes over just 3 months.
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
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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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 will consist of adults (≥18 years) with obesity (BMI ≥27 kg/m²) who are prescribed semaglutide or tirzepatide for obesity management according to routine clinical practice. Participants will be recruited before initiating GLP-1 receptor agonist therapy at the Endocrinology and Metabolism outpatient clinic and will undergo standardized oral examinations and saliva assessments at baseline and after 3 months of treatment.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Adults aged 18 years or older. * Body mass index (BMI) ≥27 kg/m². * Clinical decision by an endocrinologist to initiate semaglutide or tirzepatide therapy for obesity management. * No previous treatment with GLP-1 receptor agonists. * Willingness to participate and ability to provide written informed consent. * Willingness to attend both the baseline and 3-month follow-up visits. Exclusion Criteria: * Previous use of any GLP-1 receptor agonist. * History of head and neck radiotherapy. * Sjögren syndrome or other systemic diseases affecting salivary gland function. * Chronic kidney disease. * Pregnancy or breastfeeding. * Use of medications known to markedly affect salivary secretion. * Active orthodontic treatment. * Severe dental erosion requiring restorative treatment at baseline. * Edentulism or the absence of anterior teeth required for dental hard tissue assessment. * Inability or unwillingness to comply with the study protocol or attend the 3-month follow-up visit. * History of eating disorders associated with recurrent self-induced vomiting (e.g., bulimia nervosa). * Medical conditions causing persistent vomiting or severe gastroesophageal disease unrelated to GLP-1 therapy.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Department of Periodontology, Bilecik Seyh Edebali University Faculty of Dentistry
Bilecik, Merkez, 11100, Turkey (Türkiye)
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