Tokyo, April 29 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061400) titled 'Association Between Glycemic Measures and Periodontal Parameters in Patients with Periodontal Disease Attending Dental Clinics: Detection of Impaired Glucose Tolerance Using Blood Glucose and HbA1c' on April 28.

Study Type: Observational

Primary Sponsor: Institute - Kagawa university

Condition: Condition - periodontal disease Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - This study aims to assess whether the presence or absence of impaired glucose tolerance is associated with periodontal disease-related clinical parameters in patients with periodontal disease attending dental clinics. Basic objectives2 - Efficacy

Eligibility: Age-lower limit - 30 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - This study will include individuals who meet all of the following criteria:

1. Individuals aged 30 years or older. 2. Individuals requiring periodontal disease treatment. Key exclusion criteria - (3) Exclusion criteria Individuals who meet any of the following criteria will be excluded from this study:

Individuals whom the investigator judges to be inappropriate for participation in this study, including those who meet any of the following conditions: a. Individuals who are already receiving treatment for diabetes. b. Individuals for whom periodontal examinations or blood glucose/HbA1c measurements cannot be safely performed due to severe systemic disease or acute illness. c. Individuals who are expected to have difficulty attending visits or undergoing examinations during the observation period, such as those planning to relocate or those with difficulty attending the clinic. d. Individuals with special oral conditions that are considered to affect the conduct of the study, such as after extensive jawbone resection or cases in which PISA/PESA measurements are not possible due to denture use. e. Individuals for whom continuation of the study is judged to be difficult for other medical or ethical reasons. Individuals who do not provide consent to participate in this study. Target Size - 160

Recruitment Status: Recruitment status - Open public recruiting Date of protocol fixation - 2025 Year 09 Month 22 Day Date of IRB - 2025 Year 09 Month 22 Day Anticipated trial start date - 2025 Year 09 Month 22 Day Last follow-up date - 2027 Year 12 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070255

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