ClinicalTrials.gg
RecruitingNCT07666126Updated Jun 26, 2026

Evaluation of the Effect of Hyperuricemia on Alveolar Bone Loss

An observational study in Periodontal Diseases, Hyperuricemia and Oxidative Stress, sponsored by Recep Tayyip Erdogan University Training and Research Hospital. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-26.

Primary conditionAlveolar Bone LossRegistry: Periodontal DiseasesReclassifiedWhy we changed it
Registry
Periodontal Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Alveolar Bone Loss
Why
  1. The study's title name Alveolar Bone Loss, a narrower term within Periodontal Diseases.
Confidence
High: the new condition is named in the study's own title. Of 46 hand-checked studies reclassified this way, 72% were exactly right and 89% in the right disease family; the registry's first term was right for 4% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Recep Tayyip Erdogan University Training and Research Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
80
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Periodontitis is a multifactorial disease characterized by chronic inflammation of the gum tissue and alveolar bone destruction, and is known to be associated with various systemic diseases. Hyperuricemia, on the other hand, is a metabolic condition characterized by increased serum uric acid levels and can affect inflammation, oxidative stress, and bone metabolism. In recent years, the relationship between hyperuricemia and periodontal diseases has been increasingly investigated, but the biological mechanisms of this relationship have not yet been fully elucidated. Therefore, this study aimed to determine whether there is a relationship between hyperuricemia and periodontitis and to reveal the possible pathophysiological mechanisms of this relationship, which are shaped by inflammation, oxidative stress, and bone metabolism.

A total of 80 individuals aged 18-65 years will be included in this clinical observational study. The periodontal status of the participants will be assessed using clinical periodontal parameters such as probing pocket depth, clinical attachment loss, plaque index, gingival index, and bleeding on probing. Participants will be divided into four groups according to their periodontal status and the presence of hyperuricemia: individuals with periodontitis and hyperuricemia, individuals with periodontally healthy and hyperuricemia, individuals with periodontitis but without hyperuricemia, and individuals with periodontally healthy and without hyperuricemia. Gingival crevicular fluid and serum samples will be taken from the participants. In these samples, receptor-mediated nuclear factor kappa B ligand, osteoprotegerin, total antioxidant status, total oxidant status, oxidative stress index, interleukin-1 beta, interleukin-10, interleukin-18, and nucleotide-binding oligomerization domain-like receptor protein 3 levels will be analyzed. This study is considered unique because it examines the relationship between hyperuricemia and periodontitis by evaluating inflammation, oxidative stress, and bone metabolism parameters together.

02

Conditions studied

  • Periodontal Diseases
  • Hyperuricemia
  • Oxidative Stress

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Keywords

  • periodontal disease
  • hyperuricemia
  • oxidative stress
  • alveolar bone loss
  • inflammation
03

In context

Alveolar Bone Loss Reclassified

318 studies on the registry are indexed under Alveolar Bone Loss; 79 are open to participants now.

This study's planned enrollment of 80 is above the median of 51 across 46 observational studies indexed under Alveolar Bone Loss.

Browse Alveolar Bone Loss studies →

Lead sponsor

Recep Tayyip Erdogan University Training and Research Hospital is the lead sponsor of 88 studies on the registry; 19 are open to participants now.

Compared within Alveolar Bone Loss, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Periodontal Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Recep Tayyip Erdoğan University Faculty of Dentistry

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

  • Being between 18 and 65 years of age
  • Being systemically healthy or diagnosed with hyperuricemia
  • Having at least 20 natural teeth
  • Being periodontally healthy or diagnosed with periodontitis

Exclusion criteria

Exclusion Criteria:

  • Diabetes, cardiovascular disease, osteoporosis, chronic kidney disease, metabolic syndrome, and obesity are systemic diseases that may affect purine metabolism.
  • Smoking
  • Pregnancy or lactation
  • Having received periodontal treatment within the last 3-6 months
  • Use of antibiotics, anti-inflammatory drugs, or uric acid-lowering drugs
  • Presence of systemic diseases that may affect purine metabolism
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
80 participants (estimated)
Patient registry
No

Groups and cohorts

  • Group 1: Individuals with periodontitis and hyperuricemia

    Other: Collection of gingival crevicular fluid (GCF) and serum samples · Other: Measurement of periodontal clinical parameters

  • Group 2: Periodontally healthy individuals with hyperuricemia

    Other: Collection of gingival crevicular fluid (GCF) and serum samples · Other: Measurement of periodontal clinical parameters

  • Group 3: Individuals with periodontitis but without hyperuricemia

    Other: Collection of gingival crevicular fluid (GCF) and serum samples · Other: Measurement of periodontal clinical parameters

  • Group 4: Periodontally healthy individuals without hyperuricemia

    Other: Collection of gingival crevicular fluid (GCF) and serum samples · Other: Measurement of periodontal clinical parameters

Interventions

  • OtherCollection of gingival crevicular fluid (GCF) and serum samples

    Serum and GCF samples will be collected from participants in the first session

  • OtherMeasurement of periodontal clinical parameters

    Periodontal clinical parameters will be measured from participants initially

06

What researchers measure

Primary outcomes

  1. Periodontal pocket depth

    The distance between the gingival margin and the base of the pocket will be measured in millimeters.

    Time frame: at baseline

  2. clinical attachment loss

    The distance between the enamel-cementum junction and the base of the pocket will be measured in millimeters.

    Time frame: at baseline

Secondary outcomes

  1. Level of interleukin-1 beta

    Interleukin-1 beta levels will be determined from gingival crevicular fluid and serum samples using the ELISA method.

    Time frame: at baseline

  2. Level of interleukin-10

    Interleukin-10 levels will be determined from gingival crevicular fluid and serum samples using the ELISA method.

    Time frame: at baseline

  3. Level of interleukin-18

    Interleukin-18 levels will be determined from gingival crevicular fluid and serum samples using the ELISA method.

    Time frame: at baseline

07

Study locations

1 of 1 sites recruiting
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

Start is estimated for Jun 2026; primary completion for Oct 2026, 3 months later.

Of 22 observational studies under Alveolar Bone Loss, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 27. This study's planned 3 months is below that.

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

Registered
Jun 8, 2026
First posted
Jun 24, 2026
StartEst.
Jun 10, 2026
Primary completionEst.
Oct 1, 2026
CompletionEst.
Oct 1, 2026
Last update
Jun 26, 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 Jun 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07666126
Lead sponsor
Recep Tayyip Erdogan University Training and Research Hospital
Responsible party
Hatice Yemenoğlu (Principal investigator, Recep Tayyip Erdogan University Training and Research Hospital) — Principal investigator
First posted
Jun 24, 2026
Start date
Jun 10, 2026 (estimated)
Primary completion
Oct 1, 2026 (estimated)
Completion
Oct 1, 2026 (estimated)
Last update
Jun 26, 2026

Study contacts

Hatice Yemenoglu
Contact
htcymnglu@hotmail.com
+905052977517

Oversight

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

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