3D Evaluation of the Lip Support in a Full-arch Implant-supported Rehabilitations

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-03-30

Study Completion Date

2024-12-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The goal of this observational study is to evaluate the impact of a full arch implant-supported prostheses in the lip support. In a complex rehabilitation cases, the process between the diagnosis and the delivery of a prostheses may lead with many clinical and laboratorial choices which influence the final design of the prosthetic work and consequently the facial profile of the patient.

The use of 3D facial scanners and advanced superimposition methodology allows the investigators to objectively measure several relevant parameters such as vertical occlusion of dimension and lip support.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Facial Scanning for Lip Support Assessment in Full Arch Implant Rehabilitations

NCT04753866

Lip Prosthesis User Soft Tissue

COMPLETED NA

Implant Rehabilitations in a Hospital Setting

NCT07332195

Patients Requiring an Implant-supported Rehabilitation Edentulous Patients Requiring an Implant-supported Rehabilitation

NOT_YET_RECRUITING

Occlusion and Disocclusion Time in Immediately Loaded Overdentures Supported by Two Splinted Versus Non Splinted Interforaminal Implants

NCT06376019

Edentulous Jaw

COMPLETED NA

Three-dimensional Assessment of Facial Alterations Induced by Dental Prostheses

NCT04050878

Soft Tissue

COMPLETED NA

Short Implants Supporting Single Crowns in the Posterior Region

NCT05081050

Dental Prosthesis Dental Implants Quality of Life

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Digital technologies have evolved exponentially in the dental medicine field endorsing a change between the conventional methods to virtually based methodologies in daily clinical and laboratorial practice.

Combining facial aspects and proportions with dento-gingival parameters are the basis when planning a new smile design and a final rehabilitationFacial surface images can be used for more predictable measurement and quantification of vertical dimension of occlusion and lip support before, during and after a full mouth rehabilitation. Besides that, the information obtained by facial scanners have a major impact in treatment planning process especially in multidisciplinary complex cases with the simulation of the treatment, identification of patient's expectations and the implementation of an effective communication tool.

The 4D-virtual patient is the future regarding the management of a patient in dental medicine, since the beginning of the process with data acquisition for the diagnosis to the definitive oral rehabilitation procedures. Similar to any methodology, it is important to understand what are the basis of the facial scanning and what protocols can obtain better results in terms of accuracy and reliability.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Digital Technology Prosthesis User Lip Oral Soft Tissue Conditions Occlusion

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Removable of the full arch implant-supported prostheses

The intervention planned will be the removal of full arch implant-supported prostheses and the acquisition of a digital image through a facial scanner before and after this moment.

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Individuals with at least a full-arch implant supported rehabilitation in the upper arch
* Individuals with a provisional or a definitive implant-supported prosthesis
* Individuals with a stable occlusion function
* Individuals with compliance to collaborate with the research protocol

Exclusion Criteria

* Individuals with history of hypersensitivity to external light or any similar condition
* Individuals in an active surgical treatment period
* Individuals in an active orthodontic treatment in the opposite arch
* Individuals in an active facial treatment
* Individuals who did not attend the maintenance visits

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes