About this trial
The anterior maxilla is a particularly challenging area for immediate implant placement due to its thin buccal bone walls. These walls are more susceptible to resorption after tooth extraction, which can lead to significant bone loss and inadequate support for an implant. However, Different socket dimension may affect the amount of bone formed labial to the implant, regardless of the garfting procedure.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Immedaite implants in anterior maxilla
thick gingival phenotype
intact but thin labial plate of bone (≤1mm)
sufficient apical bone to attain implant primary stability (a minimum of 35 Ncm insertion torque)
Disqualifiers
smokers
pregnant women
patients with systemic disease
patients with parafunctional habits such as bruxism or clenching,
Trial population
Primary care clinic
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
Immediate implants with bone grafts
Procedure/SurgeryImmediate implants with bone grafts
Immediate implant placed without bone grafts or any grafting substitutes in the labial gap
Procedure/SurgeryImmediate implant placed without bone grafts or any grafting substitutes in the labial gap
Treatment groups
Trial outcomes
Primary outcomes
Bone labial to the implant
measured at three levels 0, 2, and 5 mm below the labial bone crest after one year. Using fusion software.
Secondary outcomes
Bone area at the Interproximal component
Bone area at the mesial and distal Interproximal component in mm2
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: