Alveolar socket preservation with graft and flap surgery
Procedureteeth to either the control group (coagulant-filled alveoli) or the test group (alveoli filled with platelet-rich fibrin and LPRF leukocytes)
NCT Number: NCT07278180
Understanding, through accurate and reliable volumetric analysis, how the biomaterial (LPRF) and the thickness of the vestibular bone plate influence changes in bone volume after extraction, is essential for making clinical decisions that impact implant-supported rehabilitation.
Looking for future studies?
Notify Me21 year–70 year
All sexes
Observational
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
This prospective clinical study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki and received approval from the Research Ethics Committee of Guarulhos University, São Paulo, Brazil (CEP-UnG #. 515.153). Thirty-nine patients (24 women and 15 men), aged between 22 and 80 years, who were in overall good health, non-diabetic, periodontally healthy, non-smokers, free of blood dyscrasias, not pregnant or lactating, and requiring extraction of non-contiguous, compromised teeth due to root fractures, caries, unsuccessful endodontic treatment, root resorption, or orthodontic reasons, were enrolled.
teeth to either the control group (coagulant-filled alveoli) or the test group (alveoli filled with platelet-rich fibrin and LPRF leukocytes)
Time frame: 16 weeks
Time frame: 4 months
University of Guarulhos
Other
Assessment of the Effects of Platelet and Leukocyte-rich Fibrin on Vestibular Bone Plate Thickness on Alveolar Ridge Maintenance Through Three-dimensional Analysis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06538532
Caries Active, Caries,Dental
Cairo, Egypt
View Trial DetailsNCT05049694
Caries Active, Dental Caries
Ankara, Turkey (Türkiye)
View Trial DetailsNCT07048444
Caries Active, Caries Assessment
View Trial DetailsNCT07539064
Caries Active, Prevention
Lakewood, New Jersey, United States
View Trial Details