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The Effect of MTA and PRF Application in Periapical Lesions

Assessment of Bone Healing After MTA and PRF Application in Periapical Lesions By Using CBCT

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03743987
Enrollment
36
Registered
2018-11-16
Start date
2016-12-20
Completion date
2018-11-05
Last updated
2019-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apical Periodontitis, Wound Heal

Brief summary

A total of 40 periapical lesions from the 33 patient undergoing apical surgery were randomly selected from December 2016-November 2017. Patients were informed about the surgical procedure and signed a consent form. Groups were divided in to 4; as control, MTA (mineral trioxide aggregate), PRF (platelet rich fibrin) and MTA+PRF groups. Apical resection was performed in all groups. No other interventions were made to the control group. Routine radiographs were taken in the 1st. 3th and 6th months. In the (approximately) 12th month of the procedures computerized tomography scans were taken. Primary healing of the periapical tissues were evaluated and the outcomes were measured. Patients have still been under control for the long term outcomes of the study.

Detailed description

44 apically infected periapical lesions were decided to enroll to the study from December 2016-November 2017. However; a total of 40 periapical lesions undergoing apical surgery were recruited for the planned clinical trial in the end. The study was conducted under randomized controlled protocol. Patients were informed about the surgical procedures and signed a consent form. The anticipated outcomes, possible risks and benefits of the study as well as the alternative treatment options were explained to the patients. Groups were designed to have 10 patients in each and randomly divided into four as; control, MTA, PRF and MTA+PRF. Apical resection was performed in all groups. No other interventions were made to the control group. Routine radiographs were taken in the 1st. 3th and 6th months. In the 12th month of the procedures computerized tomography (CT) scans were taken. Primary healing of the periapical tissues were evaluated according to the volumes and the densities of the lesions. Outcomes were measured. Comparison between the initial and the last 3D CT scan volumes were made by medical image processing software (MIMICS, Belgium). Patients have still been under control for the long term outcomes of the study.

Interventions

PROCEDUREPRF group

a procedure that is used for wound healing

PROCEDUREMTA + PRF group

a procedure used to prevent or resolves apical periodontitis in combination with a procedure that is used for wound healing.

PROCEDUREcontrol group

a procedure used to prevent or resolves apical periodontitis.

PROCEDUREMTA group

a procedure used to prevent or resolves apical periodontitis.

Sponsors

Recep Tayyip Erdogan University Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Single rooted canals * Failed previous root canal treatment * Retreatment at least 1 year previously * Previous surgery with unresolved bony lesion

Exclusion criteria

* More than single rooted canals * Chronic generalized periodontitis * Any systemic disease contraindicating oral surgical procedures * Evidence of root fracture * Resorptive processes involving more than apical third of the root

Design outcomes

Primary

MeasureTime frameDescription
Radiographic success - in volume1 yearEvaluation of tomographic outcomes (differences between preoperative and postoperative volume of periapical lesions)
Radiographic success - in density1 yearEvaluation of tomographic outcomes (differences between preoperative and postoperative density of periapical lesions)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026