NCT04283981View on ClinicalTrials.gov

Comparison of Operating Room Time Length With the Use of Virtual Surgical Planning Versus Conventional Treatment of Mandible Fractures

NACompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

January 24, 2021

Primary Completion Date

October 31, 2022

Study Completion Date

November 10, 2022

Conditions
Mandibular Fractures
Interventions
DEVICE

Control group without use of VSP

The control group will include patients that undergo mandibular reconstruction via open reduction internal fixation (intraoral or extraoral approach) in standard fashion (without virtual surgical planning assistance and occlusal splint)

DEVICE

Treatment Group with use of VSP

The treatment group corresponds to patients undergoing mandibular reconstruction via open reduction internal fixation (intraoral or extraoral approach) utilizing virtual surgical planning via 3D Systems, bite registration and fabrication of occlusal splint via intraoral digital scanner, and mandibular hardware

Trial Locations (1)

77030

The University of Texas Health Science Center at Houston, Houston

All Listed Sponsors
collaborator

Stryker Instruments

INDUSTRY

lead

The University of Texas Health Science Center, Houston

OTHER

NCT04283981 - Comparison of Operating Room Time Length With the Use of Virtual Surgical Planning Versus Conventional Treatment of Mandible Fractures | Biotech Hunter | Biotech Hunter