Bone AugmentationBadly Broken Maxillary Premolars Indicated for Extraction
Investigational drug(s) / intervention(s)
collagen membranetitanium mesh
collagen membrane: augmentation of the buccal plate of bone with xenograft and collagen membrane
titanium mesh: augmentation of the buccal plate of bone with xenograft and titanium mesh
Study summary
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
Sex
ALL
Min age
21 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria:
1. Patients who have at least one remaining root or badly decayed tooth in anterior maxilla.
2. Systemically free patients (American Society of Anesthesiologists I; ASA I)
3. Patients aged from 21 to 50 years old
4. Buccal bone partial deficiency (extraction socket type II)
5. Good oral hygiene
6. Accepts the follow-up period (cooperative patients)
7. Patient accepts to provides an informed consent
Exclusion Criteria:
1. Patients with habits that may jeopardize the implant longevity and affect the results of the study such as parafunctional habits such as bruxism
2. Smokers
3. Pregnant and lactating females
Primary outcome measure(s)
Buccal bone thickness — at baseline, 6 and 12 months assessment of the Buccal bone thickness in mm using CBCT
Trial sites (1)
Facility
City
Region
Status
Faculty of oral & dental Medicine,Misr international University
Cairo
Heliopolis - Cairo
Recruiting
More Misr International University trials in Egypt
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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