Clinical Trials in Poland / NCT06920849
Active, not recruiting
Not applicable
Evaluation of the Influence of PRF (Platelet-rich Fibrin) on the Clinical Parameters and the Concentration of Selected Inflammation Mediators in GCF (Gingival Crevice Fluid) of Patients With Periodontitis
NCT06920849 · tracked via the Priya Life Science Poland tracker
Condition(s) studied
Periodontal DiseasePeriodontitis
Investigational drug(s) / intervention(s)
SRP+iPRF →SRP
SRP+iPRF: SRP (scaling and root planing) with iPRF (injectable platelet-rich fibrin)
SRP: SRP (scaling and root planing)
Study summary
Assessment of the influence of injectable platelet-rich fibrin (i-PRF) on the clinical parameters and the inflammation mediators levels in the gingival crevicular fluid (GCF) in patients with periodontitis.
Eligibility
Inclusion Criteria:
* clinical and radiological features of periodontitis in stage II, III or IV
* presence of at least 4 teeth and at least 2 pockets (localized not on the same tooth) with a depth of at least 5 mm in each quadrant
Exclusion Criteria:
* periodontal treatment within 3 months prior to the study;
* antibiotic therapy within 3 months prior to the study;
* smoking; presence of systemic diseases affecting periodontal healing, i.e.: immunosuppressive diseases, diabetes, osteoporosis, AIDS, hypertension treated with calcium channel blockers;
* use of steroids or other immunosuppressive drugs;
* coagulation disorders and use of drugs affecting its mechanisms;
* pregnant and breastfeeding women
Primary outcome measure(s)
- Assessment of the influence of injectable platelet-rich fibrin on the clinical parameters in non-surgical treatment of periodontitis. — up to 6 months after treatment procedure
PD (Pocket Depth) from the gingival margin to the bottom of the sulcus, measured in mm
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Integrated Dentistry, Medical University of Białystok | Bialystok | Poland |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06920849 on ClinicalTrials.gov ↗ ← All trials in Poland