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Clinical Trials/DRKS00031209
DRKS00031209RecruitingUnknown

Clinical prospective study on the probation of additively manufactured bite splints in direct comparison to splints made of milled PMMA - Clinical probation of 3D printed bite splints

Johann Wolfgang Goethe-Universität Frankfurt am Main0 sites30 target enrollmentStarted: May 4, 2023Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Recruiting
Enrollment
30

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomized controlled study
Masking
Blinded (masking used)

Eligibility Criteria

Ages
18 Years to Years (—)
Sex
All

Inclusion Criteria

  • Patients over 18 years of age, fully dentate or fixed prosthetic upper and lower jaw, indication for the preparation of a bite splint as a nightguard, presence of eccentric bruxism or other nocturnal parafunctions of the jaw with movement pattern - evidence by BruxCheck, no arthropathy of the temporomandibular joints requiring treatment, no planned need for dental treatment during the examination period - excluding teeth cleaning, signed consent and data protection declaration on a voluntary basis for participation in the study

Exclusion Criteria

  • Patients under 18 years of age, edentulous patients or patients treated with removable dentures, no presence of bruxism or other nocturnal parafunctions of the jaw, arthropathy of the temporomandibular joints requiring treatment, dental treatment required during the study period - with the exception of tooth cleaning, lack of consent and data protection declaration, participation in the planning and implementation of the study, Presence of alcohol or drug abuse, Uncontrolled pathological processes in the oral cavity, Mental or psychosomatic illness that would affect participation in the study and compliance with the study protocol.

Investigators

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