Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05216874
Other study ID # laterognathia MPI
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 13, 2022
Est. completion date January 20, 2023

Study information

Verified date February 2022
Source Bezmialem Vakif University
Contact Kiliç
Phone +905322432756
Email bkilic@bezmialem.edu.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 48
Est. completion date January 20, 2023
Est. primary completion date August 20, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Device:
Oclusal Splint
Cl III Laterognati volunteer group using occlusal stabilization splint before orthognathic surgery -Splint will be used for at least two months

Locations

Country Name City State
Turkey Banu Kiliç Fatih Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary MPI Records for Splint Users Difference between preoperative and intraoperative condylar positions will be observed as mm with bite records. MPI will be used in the lab to determine the difference. 12 months
See also
  Status Clinical Trial Phase
Completed NCT06452368 - Palatal Versus Buccal Protraction Using Plates Assisted With Facemask in Growing Class III Patients N/A
Completed NCT05397002 - Patient Specific Intraoral Inverted-L Osteotomy Modified With Inferior Alveolar Nerve Relocation in Corrective Mandibular Surgery N/A
Completed NCT05114642 - The Effect of Orthopedic Face Mask Use on Head Posture and Pharyngeal Airway N/A
Completed NCT03172442 - Treatment of Skeletal Class III Malocclusion Using Orthodontic Removable Traction Appliance N/A
Recruiting NCT04863404 - Evaluation of the Treatment Effects of Tooth Borne Versus Bone-anchored Protraction Procedures in Class III Patients With Maxillary Deficiency N/A
Enrolling by invitation NCT04911400 - Effects of Class III Elastics on Stability of Orthopaedic Class III Correction N/A
Completed NCT04823325 - Determining the Presence of RAP in Orthognathic Patients and Its Effect on Root Resorption by Biomarkers
Completed NCT05280678 - Success Rate of the Miniscrews in the Mandibular Buccal Shelf N/A
Not yet recruiting NCT04387175 - Intraoral Device vs Facial Mask for Class III Treatment N/A
Recruiting NCT04354116 - MARPE in Patients With Cleft Lip and Palate N/A
Completed NCT05350306 - The Effects of the Chin Cup on Temporomandibular Joint and Mandibular Dimensions N/A
Completed NCT03353116 - Assessment of Maxillary Stability in Bimaxillary Orthognathic Patients Using the Inverted Sequence Approach N/A
Completed NCT03976635 - Evaluation of Pain, Discomfort and Acceptance During the Orthodontic Treatment of Class III Malocclusion N/A
Not yet recruiting NCT04229797 - Mandibular First Molar Distalization N/A
Completed NCT04887974 - Canine Retraction With Temporary Anchorage Devices N/A
Recruiting NCT04905004 - Efficiency of Canine Retraction Using Different Reactivation Intervals N/A
Not yet recruiting NCT03085082 - Study of the Relationship Between Blood Groups,RH and Skeletal Malocclusion : a Cross Sectional Study N/A