[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tmj\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tmj":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100637183","a-double-blind-placebo-controlled-evaluation-of-the-effect-of-the-erchonia-evrl-on-chronic-jaw-pain-arising-from-tmj-100637183",false,"NCT07600203","A Double-blind, Placebo-controlled Evaluation of the Effect of the Erchonia® EVRL on Chronic Jaw Pain Arising From TMJ","A Double-blind, Placebo-controlled, Randomized Evaluation of the Effect of the Erchonia® EVRL on Chronic Jaw Pain Arising From TMJ Clinical Study Protocol","Inclusion Criteria:\n\n* Able to understand and voluntarily sign the IRB-approved informed consent form.\n* Adults 22 to 75 years of age.\n* Subject's self-reported rating for jaw pain on the 0-100 VAS pain scale is 50 or greater (≥ 50).\n* Constant jaw pain on-going over at least the past 3 months.\n* Subjects score ≥3 points on the validated TMD Pain Screener (long version).\n* Subject has a primary diagnosis of TMJ-related nociceptive musculoskeletal pain made by a suitably qualified healthcare professional, confirmed using the Diagnostic Criteria for Temporomandibular Disorders (DC\u002FTMD) Axis I, with at least one of the following pain-related diagnoses: myalgia (including local myalgia, myofascial pain, myofascial pain with spreading, myofascial pain with referral) and\u002For arthralgia.\n* Subject is willing and able to refrain from consuming any OTC and\u002For prescription medications including muscle relaxants and\u002For herbal supplements and\u002For recreational and medical drugs including cannabis intended for the relief of pain and\u002For inflammation throughout the course of study participation, except for the study-specific pain relief medication of OTC Tylenol.\n* Subject agrees to refrain from taking a dosage of the study rescue pain medication of over-the-counter Regular Strength Tylenol® tablets for at least 6 hours before a scheduled VAS jaw pain rating is to be recorded. The subject understands that he may take a dosage of the over-the-counter Regular Strength Tylenol® tablets right after the VAS rating has been recorded, if needed to manage jaw pain.\n* Subject is willing and able to refrain from engaging in any non-study procedure therapies for the management of his or her jaw pain throughout the course of study participation, including conventional therapies such as physical therapy, occupational therapy and hot or cold packs, as well as alternative therapies such as chiropractic care and acupuncture\n* Subject is able to communicate fluently in English with the investigator and is able to read and write English sufficiently to comply with the study procedures.\n\nExclusion Criteria:\n\n* Pain that is undiagnosed or determined by a qualified medical\u002Fdental professional to be primarily attributable to causes other than TMJ-related nociceptive musculoskeletal pain.\n* Diagnosis using the Diagnostic Criteria for Temporomandibular Disorders (DC\u002FTMD) Axis I does not include at least one of the following pain-related diagnoses: myalgia (including local myalgia, myofascial pain, myofascial pain with spreading, myofascial pain with referral) and\u002For arthralgia OR includes one or more of the following pain-related diagnoses: disc displacement disorder with reduction, disc replacement disorder with reduction with intermittent locking, disc displacement disorder without reduction with limited opening, disc displacement disorder without reduction without limited opening, degenerative joint disease, headache attributed to RMD, and subluxation.\n* History of surgical intervention involving the temporomandibular joint within the past 12 months, or any history of total joint replacement or major reconstructive surgery of the TMJ.\n* Intra-articular TMJ interventions, including corticosteroid injections, botulinum toxin injections, or prolotherapy, within 3 months prior to enrollment.\n* Neurologic, neuromuscular, or neuropathic conditions affecting the craniofacial region that could confound TMJ pain assessment, including:\n\n  1. Diagnosed conditions: trigeminal neuralgia, Parkinson's disease, or other neuropathic facial pain disorders\n  2. Pain primarily characterized by neuropathic descriptors (burning, shooting, electric-like, sharp\u002Fstabbing pain, paresthesias, numbness, or tingling).\n* TMJ ankylosis or severe structural deformity requiring surgical intervention.\n* Degenerative disc disease or internal derangement of the temporomandibular joint associated with significant structural degeneration, disc perforation, or requiring surgical intervention.\n* Diagnosed systemic inflammatory or autoimmune conditions that could confound pain assessment (e.g., active rheumatoid arthritis, lupus) unless stable and well controlled.\n* Active cancer or treatment for cancer in the past 6 months.\n* Active infection, wound, or other external trauma to the areas to be treated with the laser.\n* Medical, physical, or other contraindications for, or sensitivity to, light therapy.\n* Pregnant, breast feeding, or planning pregnancy prior to the end of study participation.\n* Serious mental health illness such as dementia or schizophrenia; psychiatric hospitalization in past two years.\n* Developmental disability or cognitive impairment that in the opinion of the investigator would preclude adequate comprehension of the informed consent form and\u002For ability to record the necessary study measurements.\n* Any condition or other variable that in the opinion of the investigator may confound or interfere with the evaluation of the effectiveness of the investigational treatment or otherwise render the subject unable to comply with the requirements of the study protocol.","ALL","22 Years","75 Years",{"count":20,"type":21},64,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this clinical study is to determine the effectiveness of the Erchonia EVRL, manufactured by Erchonia Corporation (the Company), in providing temporary relief of nociceptive musculoskeletal chronic jaw pain arising from temporomandibular joint (TMJ).",[27,28,29],"TMJ","TMJ Pain","TMD","RECRUITING","2026-05-14",{"date":33,"type":34},"2026-05-20","ACTUAL",{"date":31,"type":34},{"date":37,"type":21},"2027-12-22",{"name":39,"class":40},"Erchonia Corporation","INDUSTRY",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":16,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":41},"100473010","application-of-a-dental-dedicated-mri-in-the-diagnosis-of-temporomandibular-joint-disorders-tissue-alterations-related-to-third-molars-periapical-and-periodontal-inflammatory-diseases-and-implant-treatment-planning-100473010","NCT05439330","Application of a Dental-dedicated MRI in the Diagnosis of Temporomandibular Joint Disorders, Tissue Alterations Related to Third Molars, Periapical and Periodontal Inflammatory Diseases, and Implant Treatment Planning","Application of a Dental-dedicated MRI in the Diagnosis of Temporomandibular Joint Disorders, Tissue Alterations Related to Third Molars, Periapical and Periodontal Inflammatory Diseases, and Implant Planning","Inclusion Criteria (one of the following):\n\n* referred for CBCT imaging of at least one tooth for endodontic reasons\n* referred for intra-oral and\u002For panoramic imaging covering at least one molar tooth for periodontal reasons\n* referred for CBCT imaging of the TMJ (bilaterally)\n* referred for panoramic imaging of the third molar (retained\u002Fsemi-retained, uni- or bilateral), prior to treatment planning\n* referred for CBCT imaging prior to implant treatment\n\nExclusion Criteria:\n\n* younger than 18 years\n* unable to give consent\n* pregnant\n* pronounced claustrophobia\n* pacemakers or implanted defibrillators\n* metal shrapnel injuries of the eyes or MRI incompatible metallic inclusions or implants large tatoos\n* non-removable piercings",true,"18 Years",{"count":52,"type":21},470,[24],"The aim of the present study is to show that the use of 0.55T MRI combined with a \"dental\" coil produces images of sufficient diagnostic value to assess areas of interest in dentistry, and to compare MR images to traditional, dental-oriented radiographic images for diagnostic purposes.",[27,56,57,58,59],"Apical Periodontitis","Periodontal Inflammation","Retained Tooth","MRI","2026-04-28",{"date":62,"type":34},"2026-05-04",{"date":64,"type":34},"2022-09-01",{"date":66,"type":21},"2026-12-31",{"name":68,"class":69},"University of Aarhus","OTHER",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":41},"100609219","treatment-of-temporomandibular-joint-disorders-with-a-stabilizing-occlusal-splint-in-somatosensory-tinnitus-100609219","NCT07211711","Treatment of Temporomandibular Joint Disorders With a Stabilizing Occlusal Splint in Somatosensory Tinnitus","Treatment of Temporomandibular Joint Disorders With a Stabilizing Occlusal Splint in Somatosensory Tinnitus: a Randomized Double-blind Placebo-controlled Clinical Trial","Inclusion Criteria:\n\n* Patients over 18 years old;\n* Sufferers of somatosensory tinnitus and TMD for more than 6 months;\n* Dentition in good health, with at least minimal occlusion up to the second premolars on both sides;\n* Availability for at least 4 months of follow-up;\n* Able to speak and read the Portuguese language.\n\nExclusion Criteria:\n\nPregnant patients; Treatment for TMD in the last 3 months; Treatment for tinnitus in the last 3 months; Use of total or partial removable prostheses Presence of orofacial pain disorders not related to TMD; Medical contraindication to treatment; Reluctance to accept any designated treatment; Unable or unwilling to give informed consent; Language barrier or delay in neuropsychomotor development.",{"count":78,"type":21},63,[24],"This clinical trial aims to investigate whether treatment of temporomandibular joint disorder with a stabilizing occlusal splint is justified to alleviate somatosensory tinnitus. The main questions we aim to answer are:\n\n* Determine if treatment of temporomandibular disorder with a stabilizing occlusal splint improves somatosensory tinnitus.\n* Identify which patient-related, tinnitus-related, and temporomandibular disorder-related factors contribute to the therapeutic effect.",[82,27,83],"Tinnitus","Temporomandibular Disorders (TMD)",[85,86,29,87,27,88,89,90,91,92],"tinnitus","temporomandibular disorders","temporomandibular joint","bite splint","occlusal splint","splint","stabilizing splint","somatosensory tinnitus","2025-09-30",{"date":95,"type":34},"2025-10-08",{"date":97,"type":34},"2023-08-10",{"date":99,"type":21},"2026-06-30",{"name":101,"class":69},"University of Sao Paulo General Hospital"]