REPLACEPatient Perception and Oral Function of Implant-supported Restorations for Posterior Teeth
This study aims to evaluate the patient's perception and oral function of implant-supported restorations for posterior teeth, focusing on changes in marginal bone loss, oral function, and oral health related quality of life.
Splinted
Bites and Stings+1
+ Poisoning
+ Wounds and Injuries
Treatment Study
Summary
Study start date: March 1, 2024
Actual date on which the first participant was enrolled.This clinical trial investigates how different dental treatments affect chewing ability and overall oral health quality of life for people missing back teeth. The study aims to determine whether implant-supported crowns, removable dental prostheses, or no treatment affect patients' perceptions of their chewing function and oral health differently. It also compares two digital methods for assessing how teeth come together and whether crowns that are joined together (splinted) or used individually (non-splinted) lead to different biological and technical outcomes. The study targets adults who are in good health, have missing back teeth, and are considering implant-supported crowns to replace these teeth. This research is significant as it may help improve dental care by identifying the most effective and patient-friendly treatment options for those with missing teeth. Participants will undergo various tests and procedures during the study. Initially, they will be screened with X-rays and other assessments to ensure they meet the study criteria and do not have conditions that could interfere with treatment. Participants will receive implant-supported crowns and undergo tests to measure their bite force, chewing time, and muscle activity during chewing. They will also complete questionnaires about their oral health and ability to chew different foods. Some participants will have their crowns joined together, while others will have them as individual units to assess the differences. Digital scans and traditional methods will be used to record how teeth meet during biting. The study will follow participants over time to assess outcomes like changes in bone levels around the implants and any complications with the crowns. This will help determine the most effective treatment approach for improving oral function and quality of life.
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 30 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.Conditions
Pathology
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
Group II
Study Objectives
Primary 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 Health and Medical Sciences
Copenhagen, DenmarkOpen Faculty of Health and Medical Sciences in Google Maps