October 6 University
Cairo, 12511, Egypt
Location status: Recruiting
Location contact
Amany A Alaraby, MD
SUB_INVESTIGATOR
Amir R Elngar, B.D.S
CONTACT
Reham L Aggour, MD
SUB_INVESTIGATOR
NCT Number: NCT07613606
This study aims to clinically and radiographically evaluate the adjunctive effect of injectable platelet-rich fibrin (i-PRF) used in combination with a minimally invasive non-surgical technique for the regenerative treatment of intrabony periodontal defects.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Cairo, 12511, Egypt
Location status: Recruiting
Amany A Alaraby, MD
SUB_INVESTIGATOR
Amir R Elngar, B.D.S
CONTACT
Reham L Aggour, MD
SUB_INVESTIGATOR
Periodontitis is a chronic inflammatory disease characterized by the progressive destruction of the periodontal supporting tissues, ultimately leading to tooth loss if left untreated.
Optimal periodontal regeneration within intrabony defects depends on the preservation of soft tissues and the maintenance of primary wound closure. Minimally invasive non-surgical periodontal therapy (MINST) has been introduced as a concept aiming to obtain extensive subgingival debridement with minimal tissue trauma.
Platelet-rich plasma (PRP) is an autologous blood product which is created through the centrifugation process of whole blood. It is defined as having a platelet concentration above that of normal physiological levels. The platelets present in PRP carry granules containing a significant number of active biomolecules.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will receive minimally invasive non-Surgical technique (MINST) alone
Patients will receive minimally invasive non-Surgical technique (MINST)+ injectable platelet-rich fibrin (i-PRF) injection
Time frame: 6 months postoperatively
Assessment of intrabony defect fill radiographically will be measured using the standardized paralleling technique.
Presence of comparable bilateral-walled intrabony defects (PPD, > 5 mm with intrabony defect depth ≥ 3 mm, from the alveolar crest to the defect base, at screening radiograph) not in a furcation-involved tooth.
Time frame: 6 months postoperatively
Clinical attachment level (CAL) will be measured in millimeters from the cemento-enamel junction (CEJ) to the base of the periodontal sulcus at 6 sites per tooth
Time frame: 6 months postoperatively
Probing depth (PD) will be measured in millimeters from the gingival margin to the base of the periodontal sulcus at 6 sites per tooth
Time frame: 6 months postoperatively
Gingival margin will be measured from the cemento-enamel junction (CEJ).
Time frame: 6 months postoperatively
Bleeding on Probing (BoP) will be measured using papillary bleeding index that is induced by gentle manipulation of the tissue at the depth of the gingival sulcus
Time frame: 6 months postoperatively
Plaque index (PI) will be measured for estimating the status of oral hygiene by measuring dental plaque that occurs in the areas adjacent to the gingival margin
Contact information is provided by the study sponsor or research team.
October 6 University
Other
Injectable Platelet-Rich Fibrin (i-PRF) With Minimally Invasive Non-Surgical Technique in Treatment of Periodontal Intrabony Defects: A Randomized Clinical Trial
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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.
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