ClinicalTrials.gg
RecruitingNCT07890389Updated Oct 22, 2026

Dynamic vs. Static Jaw Relations in Implant-Supported Prostheses: Chewing Efficiency

An interventional study of Conventional Static Jaw Relation Registration and Dynamic Digital Jaw Tracking Registration in Chewing Efficiency in Completely Edentulous Patients Rehabilitated With Implant-Supported Full-Arch Prostheses, sponsored by Mansoura University. Recruiting at 1 site in Egypt. Open to participants aged 40 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Mansoura University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Updated Oct 22, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Non-randomized
Ages
40 Years to 70 Years
Sex
All
01

Study summary

This study aims to compare the chewing efficiency of implant-supported full-arch prostheses fabricated using two different jaw relation registration techniques: conventional static jaw relation registration and dynamic jaw tracking.

Ten completely edentulous patients will be recruited from the Department of Removable Prosthodontics, Faculty of Dentistry, Mansoura University. Each participant will receive implant-supported full-arch prosthetic rehabilitation according to the All-on-6 concept. Two definitive zirconia prostheses will be fabricated for each participant, one using conventional static jaw relation records and the other using dynamic jaw tracking records, in a crossover study design.

Chewing efficiency will be evaluated using a two-color chewing gum mixing test at the time of definitive prosthesis insertion, three months after insertion, and six months after insertion. The degree of color mixing will be analyzed using dedicated image-analysis software.

The study will investigate whether dynamic jaw relation registration provides different chewing efficiency outcomes compared with the conventional static technique in patients rehabilitated with implant-supported full-arch prostheses.

Read the detailed description

**Background**

Conventional complete dentures are widely used to rehabilitate completely edentulous patients; however, they may not fully restore masticatory function because of limitations in retention, stability, and supporting tissue conditions. Implant-supported full-arch prostheses provide an alternative rehabilitation option that can improve prosthesis stability, oral function, and patient satisfaction.

Accurate registration of the maxillomandibular relationship is an important component of prosthodontic treatment. Conventional jaw relation registration relies on clinical records, occlusion rims, and articulator-based procedures. Digital jaw tracking systems allow recording of mandibular movements and may facilitate the development of prostheses that better reflect individual mandibular dynamics. However, the effect of dynamic jaw relation registration on chewing efficiency in patients receiving implant-supported full-arch prostheses requires further clinical investigation.

**Objective**

The primary objective is to compare chewing efficiency between implant-supported full-arch zirconia prostheses fabricated using conventional static jaw relation registration and those fabricated using dynamic digital jaw tracking.

**Study Design**

This study will use a crossover clinical design involving ten completely edentulous patients recruited from the Department of Removable Prosthodontics, Faculty of Dentistry, Mansoura University.

**Participants**

Eligible participants will have completely healed residual alveolar ridges, a Class I maxillomandibular relationship, sufficient restorative space, and adequate bone dimensions in the planned implant placement areas. Patients with systemic disorders affecting bone healing, contraindications to surgery, a history of head and neck radiotherapy or chemotherapy, poor neuromuscular coordination, temporomandibular joint dysfunction, or parafunctional habits will be excluded.

**Interventions and Procedures**

Participants will receive conventional complete dentures initially. A radiographic guide and a computer-designed surgical guide will be fabricated using a dual-scan protocol to facilitate implant planning and placement according to the All-on-6 concept in the maxilla and mandible, subject to clinical and radiographic assessment.

After implant placement and completion of the required healing and prosthetic procedures, digital implant impressions will be obtained using intraoral scanning.

Two jaw relation registration approaches will be used:

  1. **Conventional static jaw relation registration:** Maxillary and mandibular record bases and occlusion rims will be used to record the vertical dimension of occlusion and centric relation. A facebow transfer and semi-adjustable articulator will be used for mounting and articulator adjustment.
  2. **Dynamic digital jaw relation registration:** A central bearing device attached to the record bases and a digital jaw tracking system will be used to record mandibular movements and jaw relations.

Two definitive zirconia prostheses will be fabricated for each participant using the respective jaw relation registration technique. The order of assessment and prosthesis use will follow the finalized crossover protocol.

**Outcome Assessment**

The primary outcome will be chewing efficiency, assessed using a two-color chewing gum mixing test. Participants will chew the test material for specified numbers of chewing strokes. The flattened specimens will be analyzed using ViewGum software to quantify color mixing.

Measurements will be performed at the time of definitive prosthesis insertion (T0), three months after insertion (T3), and six months after insertion (T6), according to the finalized study protocol.

**Statistical Analysis**

Data will be analyzed using SPSS software, version 26. Quantitative data distribution will be assessed using the Shapiro-Wilk test. Normally distributed data will be summarized as mean and standard deviation, while non-normally distributed data will be summarized using the median and an appropriate measure of dispersion. Statistical tests appropriate for the crossover design, repeated measurements, and distribution of the data will be used. Statistical significance will be set at p ≤ 0.05.

02

Conditions studied

  • Chewing Efficiency in Completely Edentulous Patients Rehabilitated With Implant-Supported Full-Arch Prostheses

Keywords

  • Chewing efficiency
  • Dynamic jaw relation
  • Static jaw relation
  • Jaw tracking
  • Crossover study
03

In context

Lead sponsor

Mansoura University is the lead sponsor of 1,114 studies on the registry; 185 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

**Inclusion Criteria**

  1. Completely edentulous patients with fully healed residual alveolar ridges.
  2. Angle's Class I maxillomandibular relationship.
  3. Sufficient maxillary and mandibular restorative space, with a minimum of 15 mm, assessed using a tentative jaw relation record.
  4. Adequate bone height in the premaxillary region and anterior mandible, confirmed radiographically.
  5. Ability to understand the study procedures and provide written informed consent.

**Exclusion Criteria**

  1. Systemic disorders affecting bone metabolism or healing, including uncontrolled diabetes mellitus and osteoporosis.
  2. Local or systemic contraindications to implant surgery.
  3. History of chemotherapy or radiotherapy to the head and neck region.
  4. Poor neuromuscular coordination.
  5. Temporomandibular joint dysfunction

    .

  6. Parafunctional habits.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    Conventional Static Jaw Relation Registration

    Participants will undergo conventional static jaw relation registration for the fabrication of an implant-supported full-arch zirconia prosthesis. Maxillary and mandibular record bases and occlusion rims will be used to record the vertical dimension of occlusion and centric relation. A facebow transfer and semi-adjustable articulator will be used for mounting and articulator adjustment. Chewing efficiency will be evaluated using a two-color chewing gum mixing test at the prespecified assessment time points.

    Procedure: Conventional Static Jaw Relation Registration

  • Experimental
    Dynamic Digital Jaw Tracking Registration

    Participants will undergo dynamic jaw relation registration using a digital jaw tracking system for the fabrication of an implant-supported full-arch zirconia prosthesis. Digital impressions will be obtained using an intraoral scanner, and mandibular movements will be recorded using a jaw tracking device with a central bearing device attached to the intraoral record bases. Chewing efficiency will be evaluated using a two-color chewing gum mixing test at the prespecified assessment time points.

    Device: Dynamic Digital Jaw Tracking Registration

Interventions

  • ProcedureConventional Static Jaw Relation Registration

    Conventional static maxillomandibular relationship registration for the fabrication of an implant-supported full-arch zirconia prosthesis. Maxillary and mandibular record bases and occlusion rims will be used to record the vertical dimension of occlusion and centric relation. A facebow transfer and semi-adjustable articulator will be used for maxillary cast mounting and articulator adjustment. Chewing efficiency will be evaluated using a two-color chewing gum mixing test at the prespecified assessment time points.

  • DeviceDynamic Digital Jaw Tracking Registration

    Dynamic digital maxillomandibular relationship registration for the fabrication of an implant-supported full-arch zirconia prosthesis. Digital impressions of the maxillary and mandibular arches will be obtained using an intraoral scanner. A digital jaw tracking device and a central bearing device attached to the record bases will be used to record mandibular movements and dynamic jaw relations. Chewing efficiency will be evaluated using a two-color chewing gum mixing test at the prespecified assessment time points.

06

What researchers measure

Primary outcomes

  1. Chewing Efficiency Assessed by Two-Color Chewing Gum Mixing Test

    Chewing efficiency will be assessed using a two-color chewing gum mixing test. Participants will chew two differently colored chewing gums, and the resulting specimens will be flattened to a standardized thickness and analyzed using ViewGum software to quantify color mixing. Chewing efficiency will be compared between implant-supported full-arch prostheses fabricated using conventional static jaw relation registration and dynamic digital jaw tracking. The analysis will follow the prespecified scoring method, with the measurement scale and interpretation defined in the study protocol.

    Time frame: At definitive prosthesis insertion (T0), 3 months after insertion (T3), and 6 months after insertion (T6).

07

Study locations

1 of 1 sites recruiting
  • Faculty of Dentistry, Mansoura University
    Al Mansurah, Dakahlia Governorate, Egypt
    Recruiting
08

References and documents

Publications

  • Srinivasan M, Kamnoedboon P, Angst L, Muller F. Oral function in completely edentulous patients rehabilitated with implant-supported dental prostheses: A systematic review and meta-analysis. Clin Oral Implants Res. 2023 Sep;34 Suppl 26:196-239. doi: 10.1111/clr.14068. PubMed 37750517 ↗
  • Park MH, Son K, Jin MU, Kim SY, Lee KB. Comparison of interference from eccentric movements of dental crowns fabricated via dynamic jaw motion tracking and conventional methods: a double-blind clinical study. J Adv Prosthodont. 2025 Feb;17(1):36-46. doi: 10.4047/jap.2025.17.1.36. Epub 2025 Feb 24. PubMed 40061024 ↗
  • Abdelghany AA, Fouad MM, Emera RMK, Askar O, Yaseen AAM. Impact of mandibular 4-implant overdenture base construction techniques on assessment of occlusion with digital occlusion analysis system (clinical crossover study). BMC Oral Health. 2025 May 30;25(1):853. doi: 10.1186/s12903-025-06228-3. PubMed 40448094 ↗
  • Srinivasan M, Berisha F, Bronzino I, Kamnoedboon P, Leles CR. Reliability of a face scanner in measuring the vertical dimension of occlusion. J Dent. 2024 Jul;146:105016. doi: 10.1016/j.jdent.2024.105016. Epub 2024 Apr 26. PubMed 38679136 ↗
  • Grande F, Lepidi L, Tesini F, Acquadro A, Valenti C, Pagano S, Catapano S. Investigation of the precision of a novel jaw tracking system in recording mandibular movements: A preliminary clinical study. J Dent. 2024 Jul;146:105047. doi: 10.1016/j.jdent.2024.105047. Epub 2024 May 6. PubMed 38719134 ↗

Individual participant data

Plan to share: No — Individual participant data will not be shared with other researchers. The study data will be used for the purposes of the present research, and the findings will be reported in aggregate form to protect participants' privacy and confidentiality. No individual participant data sharing is planned.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Aug 2026 (actual). Primary completion is estimated for Feb 2027, 6 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 16, 2026
First posted
Oct 22, 2026
StartActual
Aug 19, 2026
Primary completionEst.
Feb 19, 2027
CompletionEst.
Feb 19, 2027
Last update
Oct 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07890389
Responsible party
Sponsor
First posted
Oct 22, 2026
Start date
Aug 19, 2026
Primary completion
Feb 19, 2027 (estimated)
Completion
Feb 19, 2027 (estimated)
Last update
Oct 22, 2026

Study contacts

Muthanna B Ali, B.D.S
Contact
drmuthana16@gmail.com
+201551572571

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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