Effect of Functional Treatment on Mandibular Asymmetric Growth
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|ClinicalTrials.gov Identifier: NCT01113177|
Recruitment Status : Completed
First Posted : April 29, 2010
Last Update Posted : November 9, 2010
|Condition or disease||Intervention/treatment|
|Temporomandibular Joint Disorder||Device: Distraction splint therapy|
|Study Type :||Observational|
|Actual Enrollment :||22 participants|
|Official Title:||Effect of Functional Treatment on Mandibular Asymmetry Caused by Unilateral Temporomandibular Joint Involvement in Children With Juvenile Idiopathic Arthritis|
|Study Start Date :||June 1994|
|Actual Primary Completion Date :||September 2010|
|Actual Study Completion Date :||October 2010|
Distraction splint therapy
All JIA patients with asymmetric mandibular growth due to unilateral TMJ arthritis are offered non-surgical functional orthodontic splint therapy with a distraction splint. Mandibular growth is thereafter evaluated in the affected side compared with the mandibular growth in the healthy side of the same individual.
Device: Distraction splint therapy
After the diagnosis of unilateral TMJ arthritis with clinical asymmetric mandibular growth deviations the JIA patients are offered treatment with a distraction splint. The appliance consists of an acrylic splint (distraction splint) covering the occlusal surfaces of the teeth in the upper or lower dental arch. The height of the splint is thereafter gradually increased every 6th to 10th weeks in order to optimize the mandible growth in the affected side and thereby reduce the overall asymmetric mandibular growth pattern(non-surgical distraction of the TMJ and mandibular condyle).
Other Name: functional appliance
- Mandibular growth in children with unilateral TMJ arthritis treated with an acrylic distraction splint [ Time Frame: average treatment with splint is 6.4 years ]The craniofacial dimensions are measured radiologically prior to the start of the treatment with the distraction splint. Second measurements of the craniofacial dimensions are evaluated after the patients have ended the treatment with the distraction splint. In that way we are able to evaluate the craniofacial growth in the affected side compared to the craniofacial growth in the "healthy" side in JIA patients with unilateral TMJ arthritis. The succces of the distraction splint treatment is decided based the splints ability to normalize the craniofacial growth in the affacted side.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01113177
|Dep. of Orthodontics, Aarhus University|
|Aarhus, Denmark, 8000|
|Study Director:||Thomas K Pedersen, DDS Ph.D|