Using Platelet-rich Fibrin in Regenerative Endodontic Treatment in Mature Permanent Teeth

University of Medicine and Pharmacy at Ho Chi Minh City

Status

Not yet enrolling

Conditions

Periapical Abscess

Acute Apical Periodontitis of Pulpal Origin

Chronic Apical Periodontitis

Necrosis of Pulp

Treatments

Procedure: Using advanced platelet-rich fibrin (A-PRF+) or injectable platelet-rich fibrin (i-PRF) in regenerative endodontic treatment in mature permanent teeth.

Study type

Interventional

Funder types

Other

Identifiers

NCT07192289

3787/QĐ-ĐHYD

Details and patient eligibility

About

This study aims to evaluate the antibacterial effects of injectable platelet-rich fibrin (i-PRF) in vitro, and to assess the clinical and radiographic outcomes of using advanced platelet-rich fibrin (A-PRF+) and i-PRF in regenerative endodontic treatment of mature permanent teeth with necrotic pulp. The study will compare the effectiveness of PRF-based treatment with conventional blood clot-based regenerative endodontics.

Full description

This study aims to evaluate the antibacterial effects of injectable platelet-rich fibrin (i-PRF) in vitro, and to assess the clinical and radiographic outcomes of using advanced platelet-rich fibrin (A-PRF+) and i-PRF in regenerative endodontic treatment of mature permanent teeth (single-rooted teeth with necrotic pulp, with or without periapical pathology). The study will compare the effectiveness of PRF-based treatment with conventional blood clot-based regenerative endodontics.

Enrollment

57 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Participants had a single-rooted tooth with necrotic pulp (negative response to electric pulp testing), with or without periapical pathology (acute apical periodontitis of pulpal origin, chronic periapical periodontitis, periapical abscess with sinus, periapical abscess without sinus), and gave their consent to participate in the study.

Exclusion Criteria: Study samples will be excluded if any of the following criteria are met:

The tooth has had previous endodontic treatment.
The root apex is not fully developed, or there is root resorption/cracking/fracture.
The tooth has severe tooth loss and is indicated for extraction, or is indicated for restoration with a post or cast core after endodontic treatment.
The root canal is calcified.
The root canal curvature is greater than 25º.
The tooth has a periapical cyst or is associated with a jawbone cyst.
The tooth has a periodontal pocket deeper than 4 mm.
The tooth has no occlusal contact.
The patient is pregnant.
The patient has diabetes or HIV or other immunocompromised conditions.