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CompletedNCT03516201Updated Jan 27, 2026

Oral Health in Bariatric Patients

An observational study in Adiposity, Dental Diseases and Bariatric Surgery Candidate, sponsored by University of Göttingen. Completed at 1 site in Germany. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-27.

Sponsored by University of Göttingen · Observational

Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
61
Ages
18 Years and older
Sex
All
01

Study summary

As few is known about the oral health of bariatric patients, this study aimed to analyze the prevalence and severity of erosive tooth wear, dental caries and periodontal diseases of obese patients who underwent bariatric surgery in comparison to obese patients without bariatric procedures.

Read the detailed description

The prevalence of overweight and obesity is increasing since the 1980s. Being associated with several risk factors such as hypertension, hyperinsulinemia and hyperlipidemia, obesity presents an immediate and long-term health risk for diabetes mellitus, heart diseases, osteoarthritis and certain forms of cancer. For the control of obesity several therapy options have been developed: Beside conservative treatments including change of diet and lifestyle, bariatric surgery is considered as a promising option for patients with severe obesity (BMI ≥ 40 kg/m2). Allowing impressive weight loss from 40 to 80% and effective reduction of comorbidities, bariatric surgery shows some negative/adverse effects as well, like kidney problems, hyperparathyroidism, anemia and metabolic bone diseases. For oral health, two facts are particularly important to consider: Firstly, chronic regurgitation reaching the oral cavity is an important risk factor for erosive tooth wear which initially appear as smooth silky-shining glazed surfaces. Further progress is often associated with hypersensitivities and aesthetic deficits. Over time, often substantial loss can been observed, provoking hypersensitivities and aesthetic deficits. Secondly, depending on the type of bariatric surgery, pronounced postoperative metabolic and nutritional changes can be observed which also might influence oral health. Aim of this study is to analyze the prevalence and severity of erosive tooth wear, dental caries and periodontal diseases of obese patients who underwent bariatric surgery in comparison to obese patients without bariatric procedures.

02

Conditions studied

  • Adiposity
  • Dental Diseases
  • Bariatric Surgery Candidate

Keywords

  • bariatric surgery
  • Periodontitis
  • Caries
  • erosive tooth wear
  • Gingivitis
  • BMI
  • oral health
  • obesity
03

In context

Obesity

11,522 studies on the registry are indexed under Obesity; 2,033 are open to participants now.

This study's enrollment of 61 is below the median of 114 across 2,154 observational studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

University of Göttingen is the lead sponsor of 37 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study enrolls obese adults (Age over 18 years) with an BMI (body mass index) of at least 25 kg/m2 without or after bariatric surgery

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥ 18 years
  • ≥ 25 kg/m2 without or after bariatric surgery

Exclusion criteria

Exclusion Criteria:

  • refusal for participation
  • age \<18 years
  • \<25 kg/m2
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
61 participants (actual)
Patient registry
No

Groups and cohorts

  • obese patients after bariatric surgery

    obese adults (≥ 18 years) who underwent bariatric surgery

  • obese adultes without bariatric surgery

    obese adults (≥ 18 years) who did not underwent bariatric surgery at the time of the examination

06

What researchers measure

Primary outcomes

  1. Oral health of obese adults without bariatric surgery - attachment loss

    probing depths (mm) + recessions (mm)

    Time frame: 10-15 Minutes

  2. Oral health of obese adults without bariatric surgery - BOP

    BOP (Bleeding on probing, %) as indicator of inflammation

    Time frame: 2 Minutes

  3. Oral health of obese adults without bariatric surgery - dental caries

    ICDAS (International Caries Detection and Assessment System II, 0-6), presence of restaurations/ crowns (yes/no): calculation of DMFT

    Time frame: 2-5 Minutes

  4. Oral health of obese adults without bariatric surgery - erosive tooth wear

    BEWE (Basic erosive wear examination, 0-3)

    Time frame: 1-2 Minutes

Secondary outcomes

  1. Oral health of obese adults after bariatric surgery - attachment loss

    probing depths (mm) + recessions (mm)

    Time frame: 10-15 Min

  2. Oral health of obese adults after bariatric surgery - BOP

    BOP (Bleeding on probing, %) as indicator of inflammation

    Time frame: 2 Minutes

  3. Oral health of obese adults after bariatric surgery - dental caries

    ICDAS (International Caries Detection and Assessment System II, 0-6), presence of restaurations/ crowns (yes/no): calculation of DMFT

    Time frame: 2-5 Minutes

  4. Oral health of obese adults after bariatric surgery - erosive tooth wear

    BEWE (Basic erosive wear examination, 0-3)

    Time frame: 1-2 Minutes

07

Study locations

1 site
  • Dept. of Prev. Dentistry, Periodontology and Cariology, University Medical Center Göttingen
    Göttingen, 37075, Germany
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jun 2018 to primary completion in Feb 2020, 19 months.

Of 791 non-industry observational studies under Obesity, half reached primary completion within 40 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 106. This study's 19 months is below that.

Counting every sponsor, half of 836 studies reached it within 39 months; a quarter within 17 and three quarters within 96.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 21, 2018
First posted
May 4, 2018
StartActual
Jun 15, 2018
Primary completionActual
Feb 12, 2020
CompletionActual
Feb 12, 2020
Last update
Jan 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03516201
Lead sponsor
University of Göttingen
Responsible party
Philipp Kanzow, Prof. Dr. med. dent., Dr. rer. medic. (Postdoctoral Research Fellow, University of Göttingen) — Principal investigator
First posted
May 4, 2018
Start date
Jun 15, 2018
Primary completion
Feb 12, 2020
Completion
Feb 12, 2020
Last update
Jan 27, 2026

Study contacts

Annette Wiegand, Prof. Dr. med. dent.
study director · Dept. of Prev. Dentistry, Periodontology and Cariology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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