Menu
Recruiting NCT06875830

Comparison of Immediate Implant Placement With Titanium Mesh Versus Collagen Membrane in Type II Socket:

No phase Interventional Bone Augmentation Badly Broken Maxillary Premolars Indicated for Extraction

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: collagen membrane, titanium mesh.
Who it may be relevant to
Registry conditions: Bone Augmentation, Badly Broken Maxillary Premolars Indicated for Extraction. Basic parameters: 21 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Comparison of Flapless Immediate Implant Placement With Titanium Mesh Versus Immediate Implants Placement With Collagen Membrane in Type II Socket: A Randomized Clinical Trial

Overview

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.

Detailed description

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.

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.

Interventions

  • Procedure collagen membrane
    augmentation of the buccal plate of bone with xenograft and collagen membrane
  • Procedure titanium mesh
    augmentation of the buccal plate of bone with xenograft and titanium mesh

Primary outcome measures

  • Buccal bone thickness [Time frame: at baseline, 6 and 12 months]
Secondary outcome measures (2)
  • Soft tissue thickness [Time frame: at baseline 6 and 12 months]
  • Keratinized tissue width [Time frame: at baseline, 6 and 12 months]

Eligibility criteria

Inclusion criteria

  • 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)
  • Good oral hygiene
  • Accepts the follow-up period (cooperative patients)
  • Patient accepts to provides an informed consent

Exclusion criteria

  • 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of oral & dental Medicine,Misr international University — Cairo

Identifiers

NCT: NCT06875830 · PER5253015

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗