Evaluating healing after root-end surgery using L-PRF
Official title: Evaluation of Periapical Healing Following Endodontic Microsurgery With Leukocyte and Platelet Rich Fibrin (L-PRF)
Run by University of Pennsylvania · NCT06545084 · Data updated 2026-11-12
This study tests if using a special treatment called L-PRF during root-end surgery can help patients with ongoing tooth problems heal better and faster.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | University of Pennsylvania Academic / other |
| Locations | 1 site (Philadelphia, Pennsylvania) |
| Status | Recruiting |
| Started | August 1, 2024 |
| Main results expected | June 30, 2026 |
| Study ends | June 30, 2026 |
| Registry record updated | August 27, 2025 |
| Trial ID | NCT06545084 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults over 18 years old with persistent endodontic periapical pathology and in good general health.
✕Probably not a fit
Patients with suspected root fractures or those classified as ASA 3 or greater will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the healing of periapical tissues following endodontic microsurgery with the application of Leukocyte and Platelet Rich Fibrin (L-PRF). Patients diagnosed with persistent periapical pathology and scheduled for surgery at the University of Pennsylvania will have the option to receive L-PRF to enhance bone formation at the surgical site. Healing will be monitored through clinical and radiographic assessments at intervals of six, twelve, eighteen, and twenty-four months post-surgery.
Why it matters
Potential benefit: If successful, this approach could improve healing outcomes for patients undergoing endodontic microsurgery.
How similar studies have gone: While the use of L-PRF in dental procedures is gaining interest, this specific application in endodontic microsurgery is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Provision of signed and dated informed consent form. 2. Stated willingness to comply with all study procedures and availability for the duration of the study, including the follow-up visits. 3. Male or Female age \>18 years old. 4. In good general health (ASA 2 or less) with no contraindications for Endodontic Microsurgery. 5. Persistent endodontic periapical pathology Class A, B, or C according to the Kim and Kratchman classification (5) 6. Intact coronal restorations with no evidence of leakage or caries under the restoration. Exclusion Criteria: 1. Minors. 2. Suspected root fractures. 3. ASA classification 3 or greater. 4. Periapical pathology Class D, E, or F according to the Kim and Kratchman classification (5). 5. Patients with history of Oral or IV Bisphosphonate use. 6. Patients may be excluded if their treatment team do not believe Endodontic microsurgery and L-PRF graft is in the patient's best interests.
Where it's running
-
Penn Dental Medicine
Philadelphia, Pennsylvania, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.