Comparison of the Centric Relation Recorded by Two Methods Using Cone Beam Computed Tomography

Sponsor
Fujian Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT05512442
Collaborator
(none)
10
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2
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Study Details

Study Description

Brief Summary

The purpose of this study was to investigate and compare the variation in mandibular relation recorded by the gothic arch methods and the K7 method using cone beam computed tomography (CBCT)

Condition or Disease Intervention/Treatment Phase
  • Procedure: the centric relation
N/A

Detailed Description

ten asymptomatic participants were selected,the centric relation registrations were separately recorded according to the technique of the gothic arch method and the neuromuscular method,subsequent, they were instructed to perform CBCT wearing two bite registrations,thus using dophin software to calculate the tmj space and the upper airway and using exocad software to ananyse the mandibular position, Data were analysed with paired t-test

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparison of the Centric Relation Recorded by the Gothic Arch Methods and the Neuromuscular Method Using Cone Beam Computed Tomography
Actual Study Start Date :
Jan 1, 2020
Actual Primary Completion Date :
Mar 1, 2021
Actual Study Completion Date :
Apr 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: record the centric relation using the gothic tracing method

the vertical dimension of occlusion (VDO) were were determineded through facial appearance observation,thus,the patients were trained to execute bordering protrusive, retrusive and bilateral lateral-protrusive movements wearing the intraoral apparatus and a Gothic Arch Tracing was made, the apex of the Gothic Arch Tracing was defined as the gothic arch position.

Procedure: the centric relation
All participants were recorded the centric relation registrations according to the technique of the gothic tracing method and the neuromuscular method separately.

Experimental: record the centric relation using the neuromuscular method

the participant were subjected to a low-frequency transcutaneous electrical nerve stimulation (TENS) using the J5 Myotronics for 45 minutes,With the help of TENS, complete relaxation of the muscles were achieved and the mandibular musculature was induced to guide the mandible in the physiologic position,thus using K7 to track the physical mandibular positon which was defined as the neuromuscular position.

Procedure: the centric relation
All participants were recorded the centric relation registrations according to the technique of the gothic tracing method and the neuromuscular method separately.

Outcome Measures

Primary Outcome Measures

  1. the temporomandibular joint space [immediately]

    according to the method of Ikeda and Kawamura, tmj space measurement in sagittal of the CBCT images were performed

Secondary Outcome Measures

  1. the upper airway [immediately]

    Using the sinus/airway feature of the Dolphin software to reconstruct the upper airway,it included three region: the nasopharynx, oropharynx, and hypopharynx

Other Outcome Measures

  1. the mandibular position [immediately]

    convert the DICOM files into the exocad software and analyse the difference of the mandibular position determined by the technique of the gothic tracing method and the neuromuscular method separately.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

absence of the mandibular position Classified as ASA 1 or 2 (normal healthy patient or with mild systemic disease, according to the American Society of Anaesthesiologists Physical Status Classification System); Absence of the symptoms and signs of the temporomandibular joint; Willing to participate and to sign a written informed consent form.

Exclusion Criteria:

Cardiac pacemaker carriers and pregnant women; people with heart pace disorders and epilepsy; Temporomandibular or craniocervical disorders.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fujian Medical University Fuzhou Fujian China 350004

Sponsors and Collaborators

  • Fujian Medical University

Investigators

  • Principal Investigator: Hao Yu, Fujian Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hao Yu, Fujian Medical University, Fujian Medical University
ClinicalTrials.gov Identifier:
NCT05512442
Other Study ID Numbers:
  • 20200901
First Posted:
Aug 23, 2022
Last Update Posted:
Aug 23, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hao Yu, Fujian Medical University, Fujian Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2022