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Study identifier: NCT07666100 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of Adverse Effects Related to Prescribed Medications in a Periodontology Clinic

Condition: Having a Periodontal Prescription  ·  Sponsor: Cumhuriyet University

PhaseN/A
Planned participants571
Who can joinAll sexes, 16 Years to no upper limit
Healthy volunteersYes

About this study

Various pharmacological treatment approaches, primarily antibiotics, analgesics, and antiseptic agents, are frequently used in the treatment of periodontal diseases. While these drugs are important for the clinical effectiveness of periodontal treatment, drug-related side effects can negatively impact patient compliance, quality of life, and overall patient safety, and in some cases, may lead to premature termination of treatment. Early identification of drug-related side effects, assessment of causality, and classification of severity form the basis of pharmacovigilance practices. In this context, the Adverse Event Reporting System (FAERS), run by the United States Food and Drug Administration (FDA), is an important data source for detecting drug-related side effects and presenting safety signals. Large databases like FAERS draw attention to potential drug-related side effects and provide valuable information on drug safety. However, this data is largely based on patient/user or physician feedback, and these systems are insufficient to assess the true frequency, clinical severity, and impact on patients' quality of life of side effects. Side effects related to medications prescribed in periodontology clinics are often considered mild or transient, thus limiting systematic feedback based on real-life data. Therefore, systematic and patient-centered clinical studies using standard algorithms and scales based on real-life data are needed. This study aims to determine the frequ…

This description comes directly from the study's public registry record.

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Locations (1)

Sivas Cumhuriyet UniversitySivas, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07666100