PEEK Versus Titanium Customized Healing Abutments: Evaluation of Peri-implant Soft Tissues and Sulcus Fluid Bacterial Load
PEEK customized healing abutment
+ Titanium customized healing abutment
Treatment Study
Summary
Study start date: September 1, 2023
Actual date on which the first participant was enrolled.This study investigates the use of different materials for healing abutments, which are small connectors used in dental implants to help surrounding gum tissue heal properly. Specifically, the goal is to compare PEEK (polyetheretherketone) and titanium healing abutments in terms of their effects on the tissue around dental implants and the bacterial load in the fluid around these implants. Dental implants are used to replace missing teeth, and ensuring the surrounding tissue heals well is crucial for the implant's success and appearance. This study is important because it seeks to find if PEEK abutments, known for their biocompatibility and lower risk of bacterial build-up, could offer better healing and aesthetic outcomes compared to traditional titanium abutments. Participants in this study will receive either PEEK or titanium healing abutments after receiving dental implants. These abutments are designed to match the shape of the final tooth restoration, supporting the gum tissue as it heals. The study will measure how well the gum tissue heals and how much bacteria accumulates around the implant area. This will help determine which type of abutment provides better outcomes in terms of tissue health and cleanliness. While the study does not specify potential risks, understanding the benefits of each material can guide choices for future dental treatments, potentially leading to improved patient care and satisfaction.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.26 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 20 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
ExperimentalGroup 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 Dentistry Ain Shams University
Cairo, EgyptOpen Faculty of Dentistry Ain Shams University in Google Maps