The New Serial Treatment of Temporomandibular Disorders

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16-60
SponsorSun Yat-sen University

About this trial

The purpose of this study is to look at temporomandibular joint (TMJ) pressure as a guideline to analyze the different treatments for temporomandibular disorder (TMD), and judge the feasibility of the adjust TMJ pressure treatment and to reach a conclusion on the different treatments for different types of TMD, and determine the new serial treatment of temporomandibular disorders.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Limited Month Opening

Abnormal of the Month Opening Type

Paint During the Month Open or Close

Condylar Position Paint

Disqualifiers

Dysimmunity Disease

Dysfunction of Heart Liver and Kidney Disease

Patient can not do the Guide Line

Life-threatening Patient

Trial design

Design model

Parallel

Treatments tested in this trial

  • Adjust the TMJ Pressure to Normal Value

    Procedure/Surgery

    Adjust the TMJ Pressure by the Operation Only Once for Each Patient

  • Do not adjust the pressure of TMJ

    Other intervention

    Do the treatments normally without additional treatment

Treatment groups

4 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.

Group A: 1.Arthrocentesis onlyActive comparator 1 intervention
Group B: 3.Arthroscopic TreatmentActive comparator 1 intervention
Group C: 4.Arthroscopic with Adjust PressureActive comparator 1 intervention
Group D: 5.The TMJ Orperation TreatmentActive comparator 1 intervention
Group E: 6.The TMJ Operation with Adjust PressureActive comparator 1 intervention
Group F: 7.Bite Plate TreatmentActive comparator 1 intervention
Group G: 8.Bite Plate with Adjust pressureActive comparator 1 intervention
Group H: 2.Arthrocentesis with adjust pressureActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

all cause mortality

Time frame
24 hours

Secondary outcomes

Other outcomes

Sponsors and contacts

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