Clinical trial to assess the healing efficacy of apical periodontitis with radiolucent area using electro-magnetic apical treatment
Not Applicable
- Conditions
- Apical periodontitis
- Registration Number
- JPRN-UMIN000032698
- Lead Sponsor
- Osaka University Graduate School of Dentistry, Department of Restorative Dentistry and Endodontology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who have severe systemic diseases. Patients who have implantable medical electric devices, such as artificial cardiac pacemakers. Tooth with severe dental caries. Tooth with severe periodontitis, such as Endo-Perio lesion. Tooth with complications, internal root resorption or root fracture.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Periapical Index in a dental radiograph image 12 months after root canal obturation
- Secondary Outcome Measures
Name Time Method 1) Reduction rate of maximum diameter of bone defect in an image of cone beam computed tomography 6 months after root canal obturation 2) Periapical Index in dental radiograph images 3 and 6 months after root canal obturation 3) Presence of spontaneous pain, percussion pain, swelling, tenderness, and sinus tract 3, 6, and 12 months after root canal obturation