Dynamic Navigation for Full-Arch Dental Implants in Edentulous Patients
Nasopalatine Implants, Trans-Sinus Implants, and Trans-Nasal Implants for Full-Arch Rehabilitation
Bone Diseases+5
+ Bone Resorption
+ Stomatognathic Diseases
Treatment Study
Summary
Study start date: May 30, 2025
Actual date on which the first participant was enrolled.This study focuses on improving dental implant procedures for people who have lost all their upper teeth or have significant bone loss in their upper jaw. It explores the use of advanced technology called dynamic navigation to guide the precise placement of dental implants across the entire upper jaw. The targeted participants are adults in good general health who need full-arch dental rehabilitation. This study is important because it aims to enhance the accuracy and success rates of dental implants, potentially leading to better outcomes for patients who require these procedures. Participants in this study will undergo a series of steps to prepare for and receive dental implants. Before surgery, detailed imaging techniques like CBCT scans are used to map out the structure of the upper jaw and plan the implant placement. During the surgery, a dynamic navigation system helps guide the dental surgeon in placing the implants accurately, avoiding critical areas like nerves. After the implants are placed, patients will receive follow-up care, including medications, compresses, and dental check-ups at regular intervals to ensure healing and implant stability. The study measures the success of the implants based on their placement accuracy and overall effectiveness in dental rehabilitation.
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.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy 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