After obtaining informed consent, the study will be conducted over 2 appointments, 2-4 weeks apart.
The first appointment will focus on infection control and inflammation reduction. The canal will be instrumented with a single-file system. The canal will be then irrigated sequentially with 3% sodium hypochlorite (NaOCl), saline, and 17% ethylenediaminetetraacetic Acid (EDTA) to ensure thorough disinfection. Finally, a temporary filling of Glass Ionomer Cement will be placed over an intracanal dressing of calcium hydroxide.
At the second appointment, the final treatment will be performed based on the patient's group:
Control Group - Blood clot method for regenerative endodontics. Experimental Group 1 - Regenerative endodontics using advanced platelet-rich fibrin (A-PRF+).
Experimental Group 2 - Regenerative endodontics using injectable platelet-rich fibrin (i-PRF).
All three groups will be then sealed with mineral trioxide aggregate (MTA) and a final composite resin filling.