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Active Not RecruitingNCT06734962

Evaluation of Bone Regeneration After Apical Surgery Using Advanced Platelet-rich Fibrin: Utilization of Ultrasound for the Assessment of Periapical Lesions

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Riga Stradins University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study examines the impact of advanced platelet-rich fibrin (A-PRF) on bone regeneration in apical surgery compared to standard methods. It highlights the effectiveness of ultrasound as a diagnostic tool for assessing periapical lesions. Eligible participants were adults with specific periapical lesions following root canal treatment failures. Exclusions included patients outside specific criteria, like those with advanced periodontal disease or undergoing orthodontic treatment. Participants were randomized into two groups: one receiving A-PRF to enhance bone regeneration and a control group without it. Both groups underwent apical surgery under magnification, with different postoperative protocols. The study involved radiological and ultrasonographic evaluations of lesion size and bone healing at baseline, 6 months, and 12 months, alongside blood analyses for Vitamin D and cholesterol level to assess their potential impact on healing.

Conditions

Interventions

TypeNameDescription
PROCEDUREApical surgery procedure using A-PRFParticipants will undergo an apical surgery procedure using A-PRF. Before the surgery and at follow-ups, patients will undergo comprehensive evaluation using clinical, radiological, and ultrasonographic techniques.
PROCEDUREApical surgery without using A-PRFParticipants will undergo an apical surgery procedure without using A-PRF. Patients will undergo comprehensive evaluation before the surgery and at follow-ups using clinical, radiological, and ultrasonographic techniques.

Timeline

Start date
2021-09-12
Primary completion
2022-09-30
Completion
2025-09-30
First posted
2024-12-16
Last updated
2024-12-18

Locations

1 site across 1 country: Latvia

Source: ClinicalTrials.gov record NCT06734962. Inclusion in this directory is not an endorsement.