Comparison of Immediate Implant Placement With Titanium Mesh Versus Collagen Membrane in Type II Socket:
NCT ID: NCT06875830
Last Updated: 2026-01-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
20 participants
INTERVENTIONAL
2025-03-06
2026-09-01
Brief Summary
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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.
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Detailed Description
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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.
Materials and Methods: This parallel arm, randomized controlled clinical trial will involve systemically free patients with remaining roots or badly decayed teeth in the anterior region and buccal bone deficiency requiring implant placement. They will be randomly allocated to two equal groups. Group A (test group, n=10) will receive immediate implants (grafting with xenograft covered by titanium mesh covered by collagen membrane), while group B (test group, n=10) will receive immediate implants (grafting with xenograft covered by collagen membrane). The parameters ( buccal bone thickness \& soft tissue thickness will be assessed at 6 \& 12 months. Postoperative pain and swelling will be recorded daily by the patient for the 1st two weeks post surgically. Postoperative medication will be prescribed to the patient and postoperative instructions will be explained in detail. Follow-up will be performed to assess the parameters and to ensure performing proper oral hygiene. Data collected will be tabulated and statistically analyzed.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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immediate implant with collagen membrane
immediate implant placement will be done and augmentation of the buccal bone will be done with xenograft and collagen membrane
collagen membrane
augmentation of the buccal plate of bone with xenograft and collagen membrane
immediate implant with titanium mesh
immediate implant placement will be done and augmentation of the buccal bone will be done with xenograft and titanium mesh
titanium mesh
augmentation of the buccal plate of bone with xenograft and titanium mesh
Interventions
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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
Eligibility Criteria
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Inclusion Criteria
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
2. Smokers
3. Pregnant and lactating females
21 Years
50 Years
ALL
Yes
Sponsors
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Misr International University
OTHER
Responsible Party
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Principal Investigators
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ahmed H Farid, Masters
Role: PRINCIPAL_INVESTIGATOR
Assistant lecturer
Locations
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Faculty of oral & dental Medicine,Misr international University
Cairo, , Egypt
Countries
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Other Identifiers
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PER5253015
Identifier Type: -
Identifier Source: org_study_id
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