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Comparative Evaluation of Gnathological Function With Bruxoff®

NCT06096753 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2023-10-24

No results posted yet for this study

Summary

This study aims to compare the gnathological function of edentulous patient rehabilitated according to the full-arch method (Columbus Bridge Protocol™) with immediate loading with that of dentate patients, through at-home night-time monitoring with Bruxoff® device.

Conditions

  • Gnathological Function

Interventions

DEVICE

Bruxoff gnathological function analysis

The recordings will be carried out for 3 randomly selected nights within 3 weeks, with at least 4 hours of sleep per night.

Sponsors & Collaborators

  • Prof. Andrea Deregibus

    collaborator UNKNOWN

  • Dr. Armando Crupi

    collaborator UNKNOWN

  • Dra. Giulia Ambrogio

    collaborator UNKNOWN

  • Dr. Andrea Roccuzzo

    collaborator UNKNOWN

  • Miss Lisa Sannicolo

    collaborator UNKNOWN

  • University of Turin, Italy

    lead OTHER

Principal Investigators

  • Francesco Pera, Prof. · University of Turin, Italy

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-30
Primary Completion
2025-04-30
Completion
2025-06-30

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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 NCT06096753 on ClinicalTrials.gov