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Comparative Study of Maxillary and Mandibular Splints Used for the Treatment of Masticatory Muscle Parafunction (FEA)

NCT05007691 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2022-04-18

No results posted yet for this study

Summary

the purpose of this study is to clarify the rationale for the choice of the upper or lower jaw for positioning the occlusal splint

Conditions

  • Jaw, Edentulous
  • Mouth, Edentulous

Interventions

DEVICE

Occlusal splint

Occlusal splints are hard, made of polymer biocompatible material using digital additive technology.

Sponsors & Collaborators

  • Moscow State University of Medicine and Dentistry

    lead OTHER

Principal Investigators

  • Sergey Arutyunov, PhD · A.I. Yevdokimov Moscow State University of Medicine and Dentistry

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-16
Primary Completion
2022-02-09
Completion
2022-05-31

Countries

  • Russia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05007691 on ClinicalTrials.gov