Evaluation of Maxillary 3-implant Removable Prostheses Without Palatal Coverage on Locator Abutments
This observational study aims to evaluate the intra-oral status and condition of the prosthesis and implants in individuals using maxillary 3-implant removable prostheses without palatal coverage on locator abutments, focusing on aspects such as peri-implant health, prosthesis retention, and implant stability.
Data Collection
Collected from today forward - ProspectiveCohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: September 1, 2013
Actual date on which the first participant was enrolled.This study focuses on individuals who have received a maxillary removable full prosthesis, a type of dental implant, supported by three dental implants in a private dental clinic in Drammen, Norway. The goal is to evaluate the intra-oral status of these patients annually after implant installation and gather feedback about treatment satisfaction and daily oral functions. The implants used are made from titanium with a microrough surface, fitted with precision attachments, and the removable prostheses are made from heat cured poly-methyl-metacrylate. This research is important as it helps understand the long-term effectiveness and patient satisfaction of this specific type of dental implant procedure. Each participant will receive an invitation letter and a phone call to attend an examination visit. During this visit, they will complete a questionnaire about their general health, experiences with the implants, and any need for repair sessions in the past year. Specifically, their medical history, smoking history, and dental treatment received since implant placement will be assessed. Data will also be collected from patients' charts, including age, smoking habits, medical history, medication intake, reason for tooth loss, and the date of prosthesis insertion. The primary outcomes measured in this study include the intra-oral status, condition of the prosthesis and implants, and any biological or mechanical complications experienced during the follow-up period.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.32 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
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.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: Edentulous maxilla Competence to sign the informed consent form describing the study Exclusion Criteria: Lack of jaw bone for the placement of dental implants without the need for bone regeneration.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study 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