Status:
UNKNOWN
Comparative Evaluation of Gnathological Function With Bruxoff®
Lead Sponsor:
University of Turin, Italy
Collaborating Sponsors:
Prof. Andrea Deregibus
Dr. Armando Crupi
Conditions:
Gnathological Function
Eligibility:
All Genders
18+ years
Brief 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 pati...
Detailed Description
Dental implants are now widely used in dentistry for the rehabilitation of partially or totally edentulous arches. These devices have shown excellent clinical success and are considered a reliable lon...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Willingness to participate in the study
- Age \>18 years
- M/F sex
- Good general state of health
- Absence of clinical symptoms of bruxism, i.e. sore masticatory muscles(10,11)
- Good level of oral hygiene (assessed with FMPS \<25%)
- FMBS \<25%
- Exclusion Criteria (9):
- Age \<18 years
- Presence of severe psychiatric pathologies
- Presence of neuromuscular diseases/ severe neurodegenerative diseases
- Presence of diabetes or other metabolic diseases
- Pharmacological treatment with drugs that compromise the neuromuscular system
- Pharmacological treatment with antipsychotic drugs
- Presence of severe chronic diseases
- Cognitive disability
- Acute inflammation
- Presence of an oncological condition
- Smoking (\>10 cigarettes per day) Individuals with alcohol or drug addiction will be excluded. Subjects will also be asked not to consume caffeine, alcohol and tobacco in the 6 hours before starting the night recording with Bruxoff®(12).
- Patients with implants affected by peri-implant pathology will be excluded from the Test Group.(15) Subjects suffering from periodontal disease (Stage III/IV Grade B/C) will be excluded from the Control Group (16).
Exclusion
Key Trial Info
Start Date :
November 1 2023
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 1 2025
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT06096753
Start Date
November 1 2023
End Date
June 1 2025
Last Update
October 24 2023
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