About this trial
This study seeks to assess the clinical, radiographic, and patient-reported outcomes of root amputation 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
Severe vertical bone loss affecting only Mesio-buccal root of Maxillary molar.
Through-and-through furcation involvement
Vertical root fracture confined to a Mesio-buccal root of Maxillary molar.
Extensive root caries affecting Mesio-buccal root of Maxillary molar.
Disqualifiers
- Uncontrolled systemic disease, immunosuppression, recent bisphosphonate use, head and neck radiotherapy.
Patient non-compliance or poor oral hygiene.
Heavy smoking or inability to commit to maintenance.
Root anatomy or interradicular bone that precludes predictable root amputation; insufficient bone for implant placement that cannot be reasonably augmented.
Trial design
Parallel
Treatments tested in this trial
root amputation
Procedure/Surgeryonly one root will be amputated and the rest of the molar will be preserved
Treatment groups
Trial outcomes
Primary outcomes
regression of clinical signs and symptoms and improvement in the bone radiographically
Disappearance of signs and symptoms including tooth mobility, pain on percussion, functional success. from zero to 10 Visual analgue scale (VAS) will be used to measure the patients pain after the procedure where zero indicated no pain and 10 indicated intorable pain and the bone will be assessed Radiographically. regarding the implant 1ry and 2ndry stability using Any Check and mesiodistal radiographic bone changes.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: