Clinical Trials Directory

Trials / Completed

CompletedNCT07371078

Conventional, Additive and Subtractive Occlusal Splints for TMDs

Patient Satisfaction With Conventional, Additive and Subtractive Occlusal Splints for TMDs: A Clinical Randomized Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
27 (actual)
Sponsor
Mansoura University · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study is aiming to clinically compare between occlusal splints produced by conventional, subtractive and additive techniques in regard to patient satisfaction.

Detailed description

The development of a digital (CAD/CAM) technology incorporating three-dimensional (3D) printing and milling enabled the use of different materials and manufacturing techniques. However, it should be noted that most of the evidence is based on in vitro studies with different methodologies, limiting their validity in daily practice. To the authors knowledge, limited data in the literature clinically evaluated occlusal splints produced by conventional, subtractive and additive techniques.

Conditions

Interventions

TypeNameDescription
DEVICEConventional Stabilizing SplintManual Manufacturing
DEVICEMilled Stabilizing SplintSubtractive Manufacturing
DEVICE3D Printed Stabilizing SplintAdditive Manufacturing

Timeline

Start date
2025-02-01
Primary completion
2025-09-01
Completion
2025-12-01
First posted
2026-01-27
Last updated
2026-01-27

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07371078. Inclusion in this directory is not an endorsement.