3D-Printed vs Conventional Acrylic Stabilization Splints in Young Adults With Bruxism and Temporomandibular Disorders: A Randomized Trial

Recruiting N/A Interventional Study
Bruxism, Sleep
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 25
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
44 (estimated)
Sponsor
Baskent University · Other
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About This Trial
This randomized clinical study will compare two occlusal splint (night guard) fabrication methods in adults with bruxism (teeth grinding/clenching). Forty-four participants will be randomly allocated to receive either (1) a 3D-printed splint manufactured from a photopolymer resin (Voco V-Print) or (2) a conventional acrylic splint fabricated using standard techniques. Participants will wear the sp…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adults (≥18 years) diagnosed with bruxism (sleep and/or awake bruxism) based on clinical assessment and patient report. Indication for an occlusal splint and willingness to wear the splint during sleep for 3 months. Ability to provide written informed consent and to attend s…
Contacts

Hale Arıkan Kalaycı, Assistant Professor

+903122466666

halearikan@baskent.edu.tr

CONTACT