Skip to content

Dynamic Effect of Occlusal Vertical Dimension on Lower Facial Form and Lip Positions

Dynamic Effect of Occlusal Vertical Dimension on Lower Facial Form and Lip Positions

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07491640
Enrollment
32
Registered
2026-03-24
Start date
2026-06-01
Completion date
2026-07-31
Last updated
2026-09-11

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

Conditions

Assessment of Vertical Dimension Change

Brief summary

The purpose of this study is to evaluate the effect of increased/decreased occlusal vertical dimension (OVD) on lower facial form and lip position, to analyze variations across gender groups and to analyze variations across age groups.

Interventions

DEVICEOcclusal Vertical Dimension Modification (-4mm)

Participants will undergo fabrication and placement of removable bite splints designed to alter occlusal vertical dimension (OVD). On each side, four discrete reference points will be marked at the lowest point of the orbital margin and the highest point of the external auditory meatus using Whip-Mix reference plane marker.The subject's head position will be leveled with EZ bow laser level device and -4mm OVD color coded bite splints will be randomly placed in position. An image with desktop facial scanner will be taken.

DEVICEOcclusal Vertical Dimension Modification (-2 mm)

Participants will undergo fabrication and placement of removable bite splints designed to alter occlusal vertical dimension (OVD). On each side, four discrete reference points will be marked at the lowest point of the orbital margin and the highest point of the external auditory meatus using Whip-Mix reference plane marker.The subject's head position will be leveled with EZ bow laser level device and -2mm OVD color coded bite splints will be randomly placed in position. An image with desktop facial scanner will be taken.

DEVICEOcclusal Vertical Dimension Modification (0 mm)

Participants will undergo fabrication and placement of removable bite splints designed to alter occlusal vertical dimension (OVD). On each side, four discrete reference points will be marked at the lowest point of the orbital margin and the highest point of the external auditory meatus using Whip-Mix reference plane marker.The subject's head position will be leveled with EZ bow laser level device and 0mm OVD color coded bite splints will be randomly placed in position. An image with desktop facial scanner will be taken.

DEVICEOcclusal Vertical Dimension Modification (+2mm)

Participants will undergo fabrication and placement of removable bite splints designed to alter occlusal vertical dimension (OVD). On each side, four discrete reference points will be marked at the lowest point of the orbital margin and the highest point of the external auditory meatus using Whip-Mix reference plane marker.The subject's head position will be leveled with EZ bow laser level device and +2mm OVD color coded bite splints will be randomly placed in position. An image with desktop facial scanner will be taken.

DEVICEOcclusal Vertical Dimension Modification (+4mm)

Participants will undergo fabrication and placement of removable bite splints designed to alter occlusal vertical dimension (OVD). On each side, four discrete reference points will be marked at the lowest point of the orbital margin and the highest point of the external auditory meatus using Whip-Mix reference plane marker.The subject's head position will be leveled with EZ bow laser level device and +4mm OVD color coded bite splints will be randomly placed in position. An image with desktop facial scanner will be taken.

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Intervention model description

All participants will get all 5 sizes of splints and the order of receipt of each size will be randomized

Eligibility

Sex/Gender
ALL
Age
21 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

-Complete edentulous with complete dentures or overdentures

Exclusion criteria

* Gross facial asymmetry * A history of surgery in the facial area * A history of neurologic disorders * Ill-fitting dentures * Dentures with inaccurate occlusal vertical dimension (OVD) * Inability or unwillingness to smile * Allergy to nitrile, vinyl polysiloxane (VPS) material or photopolymer resins. * Presence of facial hair that would interfere with marking reference points on the face * Severe class II or class III malocclusion

Design outcomes

Primary

MeasureTime frame
Maxillary central incisor lengthFrom time of denture placement to about 24 hours after denture placement (depending on patient availibity)
Interlabial gap heightFrom time of denture placement to about 24 hours after denture placement (depending on patient availability)
Intercommisural widthdenture placement to about 24 hours after denture placement (depending on patient availability)
Distance from Maxillary incisal edge to upper lip in millimetersdenture placement to about 24 hours after denture placement (depending on patient availability)
Distance from Maxillary incisal edge to lower lip in millimetersdenture placement to about 24 hours after denture placement (depending on patient availability)
Upper lip lengthdenture placement to about 24 hours after denture placement (depending on patient availability)
Upper lip vermilion heightdenture placement to about 24 hours after denture placement (depending on patient availability)
Lower lip vermilion heightdenture placement to about 24 hours after denture placement (depending on patient availability)
The upper lip margin on the central incisor to the gingival margin of maxillary central incisordenture placement to about 24 hours after denture placement (depending on patient availability)
The lower lip margin on the central incisor to the gingival margin of mandibular central incisordenture placement to about 24 hours after denture placement (depending on patient availability)

Secondary

MeasureTime frame
Maxillary central incisor lengthdenture placement to about 24 hours after denture placement (depending on patient availability)
Interlabial gap heightdenture placement to about 24 hours after denture placement (depending on patient availability)
Intercommisural widthdenture placement to about 24 hours after denture placement (depending on patient availability)
Maxillary incisal edge to upper lipdenture placement to about 24 hours after denture placement (depending on patient availability)
Maxillary incisal edge to lower lipdenture placement to about 24 hours after denture placement (depending on patient availability)
Upper lip lengthdenture placement to about 24 hours after denture placement (depending on patient availability)
Upper lip vermilion heightdenture placement to about 24 hours after denture placement (depending on patient availability)
Lower lip vermilion heightdenture placement to about 24 hours after denture placement (depending on patient availability)
The upper lip margin on the central incisor to the gingival margin of maxillary central incisordenture placement to about 24 hours after denture placement (depending on patient availability)
The lower lip margin on the central incisor to the gingival margin of mandibular central incisordenture placement to about 24 hours after denture placement (depending on patient availability)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMaria D Gonzalez, DDS, MS

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 12, 2026