Efficacy of injectable platelet rich fibrin in immediate implant placement sites: A randomized controlled trial

purpose of the study is to access the efficacy of injectable platelet rich fibrin in immediate implant placement sites

Brief procedure

Atraumatic tooth extraction will be performed under local anesthesia

Extracted Socket will be assessed for Implant placement

The subjects who fulfill the inclusion criteria will be randomly assigned into following 2 groups using computer generated randomization

GROUP 1 (control group) 10 sites were treated with immediate implant placement with bone graft

GROUP 2(test group) 10 sites were treated with immediate implant placement with injectable platelet rich fibrin mixed with bone graft

The preparation of injectable platelet rich fibrin for the test group will be done by drawing 8 ml intravenous blood from the patient and collected into disposable plastic test tubes

As per Choukroun standard protocol centrifugation at 700rpm for 3min will be done

injectable platelet rich fibrin was created at upper level

It will be used along with DBM for test group

Both the groups will be assessed for clinical parameters

gingival biotype

peri implant probing depth and

radiographic parameters

marginal bone loss

peri implant radiolucency at baseline 1 4and 6months follow up