Endodontic Microsurgery With the Use of L-PRF Block
- Conditions
- Apical PeriodontitisApical Periodontal Cyst
- Interventions
- Procedure: Endodontic Microsurgery
- Registration Number
- NCT05379010
- Lead Sponsor
- Universitaire Ziekenhuizen KU Leuven
- Brief Summary
This study evaluates the effect of leucocyte and platelet rich fibrin Block (L-PRF Block) during endodontic microsurgery (EMS) on patient's post-operative comfort and periapical bone healing in large peri-apical lesions.
- Detailed Description
This study evaluates the effect of leucocyte and platelet rich fibrin Block (L-PRF Block) during endodontic microsurgery (EMS) on patient's post-operative comfort and periapical bone healing in large peri-apical lesions. The trial design is an open randomized controlled clinical trial with two groups. Half of the participants will receive EMS with L-PRF Block (experimental group), the other half without (control group).
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 20
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description With L-PRF Block Endodontic Microsurgery - No L-PRF Block Endodontic Microsurgery -
- Primary Outcome Measures
Name Time Method Amount of peri-apical bone healing 1 year Amount of periapical bone healing in time: measured with Cone Beam Computed Tomography (CBCT).
- Secondary Outcome Measures
Name Time Method Patient related outcomes 7 days Discomfort assessed with a Visual Analogue Scale ranging from 1 to 5 each day during the first 7 days post-op.
Bone or scar tissue healing 1 year Bone or scar tissue healing: Volumetric analysis using Cone-Beam Computed Tomography. Pre-operative CBCT data will be matched with the post-op CBCT scans in order to assess the volumetric changes during 1 year.
Success & survival rate 1 year Success \& survival rate
Dentinal defects 1 year Dentinal defects: in the apical root before and after resection. Potential cracks and fractures that occur during the follow-up period will be assessed on CBCT en reported.
Trial Locations
- Locations (1)
UZ Leuven
🇧🇪Leuven, Vlaams-Brabant, Belgium