About this trial
This study seeks to assess the clinical, radiographic, and patient-reported outcomes of hemisection versus implant over a 12 months period, generating robust evidence to guide clinical decision-making and enhance patient care.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Good oral hygiene and motivation for follow-up care.
Ability to understand and sign informed consent.
Localized Root/Periodontal Disease: Severe attachment loss or bone loss (e.g., severe localized periodontitis) affecting the mesial root, while the other root remains healthy.
Furcation Involvement: Class II or III furcation involvements where the disease cannot be treated by conventional methods.
Disqualifiers
Uncontrolled systemic diseases (e.g., diabetes mellitus, bleeding disorders, immunosuppression).
Fused or poorly shaped roots,
Active periodontal or endodontic infection at adjacent teeth that may interfere with treatment outcomes.
Severe bruxism or occlusal parafunction.
Trial design
Parallel
Treatments tested in this trial
hemi sectioning
Procedure/Surgeryone root will be extracted and the other root will be preserved
Treatment groups
Trial outcomes
Primary outcomes
• Regulation of clinical signs and symptoms
Patient-reported outcomes, including satisfaction, masticatory efficiency, and oral comfort measured by a visual analog scale (VAS).
Secondary outcomes
Assessment of radiographic bone changes
* Radiographic bone level changes around the retained root or implant. * Detection of any radiographic signs of pathology or treatment failure. Measurements will be recorded in millimeters (mm) using digital radiographic software calibration tools.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: