About this trial
Statement of the problem: Immediate implant placement is faced with several problems. One of the most important issues is dealing with defects in the buccal plate of bone in the esthetic zone.
Aim: The aim of this study is to assess the buccal bone thickness after augmentation with titanium mesh and xenograft upon flapless immediate implant placement.
Eligibility criteria
Qualifiers
Patients who have at least one remaining root or badly decayed tooth in anterior maxilla.
Systemically free patients (American Society of Anesthesiologists I; ASA I)
Patients aged from 21 to 50 years old
Buccal bone partial deficiency (extraction socket type II)
Disqualifiers
Patients with habits that may jeopardize the implant longevity and affect the results of the study such as parafunctional habits such as bruxism
Smokers
Pregnant and lactating females
Trial design
Treatments tested in this trial
- collagen membrane
- titanium mesh