- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06635369
Taurine in Periodontitis and Aging
October 9, 2024 updated by: Hadi Sayedyousef, Istanbul Medipol University Hospital
The Role of Taurine in Periodontitis and Aging: a Preliminary Study
Aging leads to a decline in physiological functions and increases the risk of chronic diseases.
Periodontitis is a chronic inflammatory disease that causes progressive destruction of the tissues supporting the teeth.
Taurine, an amino acid with anti-inflammatory and antioxidant effects, might impact both periodontitis and aging.
This study investigated taurine, SIRT1, and TNF-α levels in saliva and blood of 66 healthy people in different age groups, with or without periodontal disease.
The findings showed that young people with healthy periodontal status had higher levels of taurine and SIRT1 compared to others.
TNF-α, a marker of inflammation, was linked to the severity of periodontitis and may help identifying it in younger individuals.
Overall, higher TNF-α levels are associated with periodontal inflammation, while taurine levels decrease with age-related inflammation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
66
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Unkapani
-
Istanbul, Unkapani, Turkey
- Istanbul Medipol University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Exclusion Criteria:
- ages 18-25 or 45-64
- use of antibiotics, anti-inflammatory drugs, immunosuppressants, beta-blockers, calcium channel blockers, or anticoagulants within the last 6 months
- presence of diabetes, rheumatoid arthritis, or other systemic conditions such as cardiovascular, renal, hepatic, and neurodegenerative disorders
- pregnancy or lactation
- alcoholism
- smoking
- nonsurgical periodontal treatment in the past 6 months or surgical treatment in the past 12 months
- having less than 20 natural teeth, excluding third molars
- use of orthodontic appliances
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Young (25-44 years) with a healthy periodontium
|
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
|
|
Experimental: young (25-44 years) with Periodontitis
|
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
|
|
Experimental: Old (≥65 years) with a healthy periodontium
|
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
|
|
Experimental: Old (≥65 years) with Periodontitis
|
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Taurine
Time Frame: 12 Weeks
|
Taurine levels in saliva and serum were measured
|
12 Weeks
|
|
SIRT1
Time Frame: 12 Weeks
|
SIRT1 levels in saliva and serum were measured
|
12 Weeks
|
|
TNF-α
Time Frame: 12 Weeks
|
TNF-α levels in saliva and serum were measured
|
12 Weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 21, 2023
Primary Completion (Actual)
May 1, 2024
Study Completion (Actual)
June 1, 2024
Study Registration Dates
First Submitted
October 4, 2024
First Submitted That Met QC Criteria
October 9, 2024
First Posted (Actual)
October 10, 2024
Study Record Updates
Last Update Posted (Actual)
October 10, 2024
Last Update Submitted That Met QC Criteria
October 9, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1078
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Due to patients data privacy
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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