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The Effect of Splint Usage in Laterognathic Cl III Orthognathic Surgery Patients (TMJ)

B

Bezmialem Vakif University

Status

Unknown

Conditions

Laterognathia
Class III Malocclusion
Skeletal Malocclusion

Treatments

Device: Oclusal Splint

Study type

Interventional

Funder types

Other

Identifiers

NCT05216874
laterognathia MPI

Details and patient eligibility

About

It is crucial to maintain the anatomic condylar positions during orthognathic surgery. Condylar positions are affected directly under general anesthesia because of joint and muscle relaxation. Possible unwanted changes in the joint position may cause incorrect positioning of the jawbones. This could affect the success of the surgery in terms of function and facial aesthetics causing the need for a second surgery. Our aim is to evaluate whether the use of MR Splint has a statistically significant effect on muscle relaxation-induced condyle position deviations under general anesthesia in Class III Laterognathia patients.

Full description

It is crucial to maintain the anatomic condyle positions during orthognathic surgery to prevent iatrogenic temporomandibular joint complications. Condyle shunts are affected directly under general anesthesia because of the joint and muscle relaxation. Surgical guidance appliances are prepared according to the TMJ records taken chairside while patients are in an upright position. During surgery, these appliances are applied in a supine position while the muscles are relaxed. Postoperative and long-term effects of TMJ and muscle relaxation obtained under general anesthesia in class III and asymmetric patients will be examined. Patients who had occlusal splint before records taken will be evaluated in terms of condyle location by MPI.

Our aim is to evaluate whether the use of MR Splint has a statistically significant effect on muscle relaxation-induced condyle position deviations under general anesthesia in Class III Laterognathia patients.

Enrollment

48 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • being ready for orthognathic surgery
  • must be able to give centric relation records

Exclusion criteria

  • having any TMDsyndromes
  • cleft lip and palate,
  • have bruxism,
  • TMJ or muscle disfunctions,
  • under any medication of muscle relaxants,
  • narcotics and antidepressants,
  • usage of removeable prosthetics
  • have toothless areas that can affect the wax impression for centric record
  • used horizontal elastics within the last 2 months

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 2 patient groups

Occlusal stabilization splint
Experimental group
Description:
Skeletal class III laterognathia surgery patients who has occlusal stabilization splint thearapy for at least 2 mounths before surgery
Treatment:
Device: Oclusal Splint
Control
No Intervention group
Description:
Skeletal class III laterognathia surgery patients did not have occlusal stabilization splint thearapy

Trial contacts and locations

1

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Central trial contact

Kılıç

Data sourced from clinicaltrials.gov

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