Endodontic Microsurgery
Part of paid clinical trials in Lexington, Kentucky.
- Sponsor
- Mark Schachman
- Study ID
- NCT06776289
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
- Apical Periodontitis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Platelet rich fibrin — BIOLOGICALPlatelet rich fibrin will be used to fill an osteotomy after endodontic microsurgery is completed.
Study Details
Current literature on platelet rich fibrin (PRF) use in apicoectomies, also known as endodontic microsurgery, is sparse. PRF use in oral surgery or periodontal surgery has been more thoroughly researched. Whether it is able to reduce post-op pain or if it improves success rate in endodontic microsurgery is not well known. It is also not well known if it will be able to increase the rate of healing. This study will evaluate the success of endodontic microsurgery with and without PRF.
Key Dates
- Start date
- Mar 31, 2026
- Status verified
- Jan 2026
- Primary completion
- Jul 28, 2026
- Completion
- Dec 30, 2026
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Microsurgery with Platelet Rich FibrinPatents will have a blood draw completed so that PRF can be made. Endodontic microsurgery will then be completed. Prior to closing the flap, PRF will be placed in the osteotomy.
- No Intervention: Microsurgery AloneEndodontic microsurgery will be completed without PRF. The osteotomy will remain empty as per standard procedure.
Primary Outcome Measure
Change in bone deposition using voxel-based imposition [ Time Frame: 6 months, 12 months, and 18 months ]
Central Contacts
- Dawn Dawson, RDH, CCRC8593235409
- Michael Skanchy, DMD859-562-2232
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Kentucky College of Dentistry Endodontics Division | Lexington | Kentucky | 40508 |
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