Clinical and Radiographic Outcomes of PRF, Chitosan, and Blood Clot in Regenerative Endodontics of Molars
NCT07119619 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28
Last updated 2025-08-13
Summary
This clinical trial aimed to evaluate the long-term effects of using chitosan, blood clots, and platelet-rich fibrin as scaffolds in regenerative endodontics on tooth development. The trial aimed to answer the following questions:
Does chitosan shorten the duration of treatment for participants? Does chitosan promote root development? Which scaffold is most effective for root development? Which scaffold is more practical and effective to use in pediatric patients? Participants underwent regenerative endodontic treatment and were called to the clinic every six months for symptom assessment. Clinical and radiographic records were kept.
Conditions
- Regenerative Endodontics
Interventions
- PROCEDURE
-
Regenerative Endodontic Treatment Using a Blood Clot as a Scaffold
During the initial visit, the teeth were anesthetized using inferior alveolar block anesthesia. The endodontic access cavity was then opened. Each canal was irrigated with 2.5% NaOCl and saline. The canals were dried with paper points. Ca(OH)2 was placed in the canals with the objective of achieving an antimicrobial effect. After the application of root canal disinfectant, the opened cavity was sealed with a temporary filling material.The patient has been scheduled for a follow-up appointment within one to four weeks. During the second appointment, local anesthesia was performed using an anesthetic agent that did not contain a vasoconstrictor. The canals were irrigated with 17% EDTA and dried with paper points. Bleeding was induced by instrumentation with a K-type file, at 2 mm past the apical foramen, thus creating a blood clot within the canal. MTA was applied on the scaffold as capping material.
- PROCEDURE
-
Regenerative Endodontic Treatment Using a Chitosan as a Scaffold
During the initial visit, the teeth were anesthetized using inferior alveolar block anesthesia. The endodontic access cavity was then opened. Each canal was irrigated with 2.5% NaOCl and saline. The canals were dried with paper points. Ca(OH)2 was placed in the canals with the objective of achieving an antimicrobial effect. After the application of root canal disinfectant, the opened cavity was sealed with a temporary filling material. The patient has been scheduled for a follow-up appointment within one to four weeks. During the second appointment, local anesthesia was performed using an anesthetic agent that did not contain a vasoconstrictor. The canals were irrigated with 17% EDTA and dried with paper points.Chitosan in gel form was placed into the root canal space with the help of an injector.MTA was applied on the scaffold as capping material.
- PROCEDURE
-
Regenerative Endodontic Treatment Using a Platelet Rich Fibrin as a Scaffold
During the initial visit, the teeth were anesthetized using inferior alveolar block anesthesia. The endodontic access cavity was then opened. Each canal was irrigated with 2.5% NaOCl and saline. The canals were dried with paper points. Ca(OH)2 was placed in the canals with the objective of achieving an antimicrobial effect. After the application of root canal disinfectant, the opened cavity was sealed with a temporary filling material.The patient has been scheduled for a follow-up appointment within one to four weeks. During the second appointment, local anesthesia was performed using an anesthetic agent that did not contain a vasoconstrictor. The canals were irrigated with 17% EDTA and dried with paper points.Ten milliliters of venous blood was collected from the patient and immediately placed in a centrifuge at 3000 rpm for 10 minutes. The prepared PRF was placed in the canal space. MTA was applied on the scaffold as capping material.
Sponsors & Collaborators
-
Inonu University
lead OTHER
Principal Investigators
-
Beyza Sandal · Derince Oral and Dental Health Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 6 Years
- Max Age
- 14 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-02-10
- Primary Completion
- 2024-03-19
- Completion
- 2024-08-20
Countries
- Turkey (Türkiye)
Study Locations
More Related Trials
-
Platelet Rich Fibrin in the Treatment of Localized Gingival Recessions
NCT01793389 ·Status: COMPLETED ·Phase: NA
-
Effects of the Use of Platelet-rich Fibrin on Bone Regeneration After Impacted Third Molar Surgery
NCT02890680 ·Status: COMPLETED ·Phase: NA
-
Regenerative Ability of Immature Necrotic Permanent Teeth Using Different Scaffolds
NCT06693739 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
The Effect of Using Injectable Platelet-rich Fibrin on Root Surface Closure in Patients with Gingival Recession.
NCT05591326 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
The Use of Injectable Plasma Versus the Use of Simvastatin Gel in Surgical Management of Bony Defect in Dentistry
NCT04824898 ·Status: UNKNOWN ·Phase: PHASE1
-
Effect of Injectable Platelet Rich Fibrin (i-PRF) on Extraction Socket Healing: A Split-Mouth Randomized Study.
NCT07257328 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Platelet-rich Fibrin for Revascularization of Immature Permanent Teeth Versus Standard Apexification
NCT06693349 ·Status: COMPLETED ·Phase: PHASE3
-
Injectable Platelet Rich Fibrin With Collagen Matrix in Treatment of Multiple Gingival Recession.
NCT05389059 ·Status: UNKNOWN ·Phase: NA
-
Prevention of Mandibular Third Molar Extraction- Associated Periodontal Defects Using Platelet-Rich Fibrin
NCT04033744 ·Status: COMPLETED ·Phase: NA
-
Clinical and Radiographic Outcome of Regeneration in Immature Permanent Human Teeth Using a New Scaffold
NCT06812351 ·Status: COMPLETED ·Phase: PHASE1
-
Use of Injectable Extended Platelet-Rich Fibrin as a Local Drug Delivery in the Treatment of Stage II Periodontitis Patients
NCT07080294 ·Status: COMPLETED ·Phase: NA
-
Platelet-Rich Fibrin Prepared With Titanium in the Treatment of Multiple Gingival Recessions
NCT05270941 ·Status: COMPLETED ·Phase: NA
-
Comparison of the Effect of A-PRF and L-PRF on Outcomes After Removal of Impacted Mandibular Third Molar
NCT03672669 ·Status: COMPLETED ·Phase: NA
-
Regenerative Endodontic Procedure of Immature Permanent Teeth With Apical Periodontitis Using PRF
NCT02801552 ·Status: COMPLETED ·Phase: NA
-
Growth Factors in the Treatment of the Multiple Gingival Recessions
NCT05319938 ·Status: COMPLETED ·Phase: NA
-
Benefits of Platelet Rich Fibrin In Mandibular Molar Furcation Defects
NCT02430519 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Sticky Bone With or Without EDTA for Treatment of Gingival Recession
NCT04980066 ·Status: RECRUITING ·Phase: NA
-
Comparison of the Efficacy of I-Prf Impregnated Collagen and L-Prf on Healing After Impacted Third Molar Surgery
NCT05563519 ·Status: UNKNOWN ·Phase: NA
-
Clinical and Radiographic Success Following Regenerative Pulpotomy Using Chitosan Hydrogel Versus Platelet Rich Fibrin in Mature Mandibular Molars
NCT06828978 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Evaluation of Platelet Rich Fibrin on Reduction of Periodontal Problems After Surgical Removal of Mandibular Third Molar
NCT01583491 ·Status: UNKNOWN ·Phase: PHASE4
-
Efficacy of Integrated Nano-technology in Revascularization of Immature Necrotic Teeth
NCT06631885 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Comparison Between Two Regenerative Scaffolds
NCT06227533 ·Status: COMPLETED ·Phase: NA
-
Pinhole Surgical Technique for Root Coverage Using PRF
NCT04202198 ·Status: UNKNOWN ·Phase: PHASE2
-
Platelet-rich Fibrin and Connective Tissue Graft in Recession Treatment
NCT02397122 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Platelet Rich Fibrin Matrix as Regenerative Material in Intraosseous Defects
NCT03616925 ·Status: COMPLETED ·Phase: PHASE3