Evaluation of Periapical Healing Following Endodontic Microsurgery With Leukocyte and Platelet Rich Fibrin (L-PRF)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Pennsylvania

About this trial

The purpose of the study is to evaluate peri-radicular healing after root-end surgery using Leukocyte and Platelet Rich Fibrin. The study population includes patients diagnosed with persistent periapical pathology and scheduled for Endodontic Microsurgery at the University of Pennsylvania School of Dental Medicine, Department of Endodontics. Patients undergoing routine endodontic microsurgery and who meet the inclusion criteria will be given the opportunity to opt in to receive L-PRF in the osteotomy site to promote bone formation. Healing will be assessed radiographically and clinically at six, twelve, eighteen, and twenty-four months.

Eligibility criteria

Qualifiers

Provision of signed and dated informed consent form.

Stated willingness to comply with all study procedures and availability for the duration of the study, including the follow-up visits.

Male or Female age >18 years old.

In good general health (ASA 2 or less) with no contraindications for Endodontic Microsurgery.

Disqualifiers

Minors.

Suspected root fractures.

ASA classification 3 or greater.

Periapical pathology Class D, E, or F according to the Kim and Kratchman classification (5).

Trial design

Treatments tested in this trial

  • Leukocyte and Platelet Rich Fibrin

Treatment groups

No treatment groups listed

Sponsors and collaborators