Flapless Immediate Implant with Titanium Mesh vs Collagen Membrane for Anterior Teeth
collagen membrane
+ titanium mesh
Treatment Study
Summary
Study start date: March 6, 2025
Actual date on which the first participant was enrolled.This clinical trial aims to explore the effectiveness of two different methods for placing dental implants in patients who have issues with the bone in the front part of the mouth, especially where there is a deficiency in the buccal bone. The study involves patients who need implants due to roots or decayed teeth in the front area and have healthy overall conditions. One group will receive implants using a titanium mesh and a collagen membrane, while the other group will receive implants using only a collagen membrane. The goal is to determine which method better supports bone thickness and overall oral health, which can lead to improved outcomes in dental procedures. Participants in this study will undergo a procedure where implants are placed immediately after removing the damaged teeth without cutting the gum. For one group, the area will be treated with a xenograft and covered with a titanium mesh and collagen membrane, while the other group will use xenograft and collagen membrane only. The thickness of the bone and soft tissue will be measured at 6 and 12 months to evaluate success. Participants will also keep track of their pain and swelling for two weeks following the procedure. Follow-ups will ensure proper oral hygiene and medication will be provided as needed. The collected data will help identify the most effective method for implant placement.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 21 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Faculty of oral & dental Medicine,Misr international University
Cairo, EgyptOpen Faculty of oral & dental Medicine,Misr international University in Google Maps