Skip to content

Accuracy of Dental Contacts of an Occlusal Splint Made According to Conventional or Digital Techniques Using GeoMagic®.

Comparative Study of the Accuracy of Dental Contacts of an Occlusal Splint Made According to Conventional or Digital Techniques Using GeoMagic®.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05317182
Enrollment
40
Registered
2022-04-07
Start date
2022-02-17
Completion date
2022-04-30
Last updated
2022-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Occlusal Splints

Keywords

Digital Dentistry, Occlusal records, Intraoral scan

Brief summary

To compare the accuracy of the occlusal splints made by conventional impression and milled with the splint made by intraoral scanner and milled.

Detailed description

Forty participants received two different occlusal devices from two different workflows (fully conventional and fully digital). Every splint was scanned before and after the occlusal adjustments in order to compare the volumetric changes. Furthermore, the scans were compared in a software Geomagic® Control X calculates and measures the distance from every surface point from the initial dataset (occlusal devices before adjustment) to the final dataset (occlusal device after adjustment).

Interventions

OTHEROcclusal Splints Analogic-Analogic

Take a conventional impression to the patient and conventional fabrication of the splint.

OTHEROcclusal Splints Analogic-Digital

Take a conventional impression to the patient and digital fabrication of the splint.

OTHEROcclusal Splints Digital-Digital

Take a digital impression to the patient and digital fabrication of the splint.

Sponsors

Universitat Internacional de Catalunya
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

This clinical study has three arms of equal size: occlusal splints made by conventional impression and conventional fabrication (Group 1), occlusal splints made by conventional impression and digital design and fabrication (Group 2), and occlusal splints performed by intra-oral scanner and digital design and fabrication (Group 3). Otherwise, the allocation of each subject to each group will be done at random by a list made with specialized software until the sample will be fulfilled when the patient is recruited.

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients between 18 to 70 years old. * Patients who maintain until first molar in both arches. * Patients who need occlusal splints due to bruxism.

Exclusion criteria

* Pregnant patients. * Patients with removable prostheses. * Patients with fixed prostheses between six to six in both arches. * Patients with partial edentulism, do not maintain until first molar in both arches. * Patients with Temporomandibular Disorders (TMD): articular noises, pain on palpation, limited opening.

Design outcomes

Primary

MeasureTime frameDescription
Volumetric changes assessed in Root Mean Square (RMS)1 weekThe software of automatically graphical comparisons called Geomagic® Control X (Geomagic Inc., 3D Systems Inc., USA) will be used to calculate the accuracy by measuring the distance (positive or negative) from every surface point from the initial dataset (occlusal devices before adjustment) to the final dataset (occlusal device after adjustment). This approach will give us the mean of the simple arithmetic difference.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026