[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ultrasonographic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ultrasonographic":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,49,77,106,129,156],{"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":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100592600","splinting-vs-exercise-in-de-quervains-tenosynovitis-100592600",false,"NCT06995534","Splinting vs Exercise in De Quervain's Tenosynovitis","Comparison of Static Hand-Wrist Splinting and Exercise Therapy in the Management of De Quervain's Tenosynovitis","Inclusion Criteria:\n\n* Adults aged between 18 and 65 years\n\nPatients experiencing wrist pain and tenderness for less than 3 months and clinically diagnosed with acute or subacute De Quervain's tenosynovitis\n\nVisual Analog Scale (VAS) pain score ≥ 3\n\nExclusion Criteria:\n\n* History of trauma\n\nWrist fractures\n\nLocal infection\n\nPresence of rheumatologic diseases (e.g., rheumatoid arthritis, psoriatic arthritis)\n\nPresence of symptomatic hand osteoarthritis\n\nContinuous use of nonsteroidal anti-inflammatory drugs (NSAIDs) or corticosteroids\n\nReceipt of physical therapy for the hand or wrist within the past 3 months\n\nCorticosteroid injection into the hand or wrist within the past 3 months\n\nDiagnosed with significant neurological disorders (e.g., upper motor neuron disease)\n\nPresence of uncontrolled systemic diseases (e.g., uncontrolled diabetes mellitus, congestive heart failure, chronic kidney disease, hepatic failure)\n\nMajor psychiatric disorders\n\nCommunication difficulties","ALL","18 Years","65 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","De Quervain's disease is a painful tenosynovitis of the abductor pollicis longus and extensor pollicis brevis muscle tendons located in the first dorsal compartment. The primary treatment for De Quervain's disease is conservative; surgical intervention is rarely required. Currently, there is no standardized treatment protocol supported by strong, up-to-date evidence.\n\nThe aim of this study is to compare the effectiveness of a static hand-wrist resting splint and exercise therapy in the conservative treatment of De Quervain's tenosynovitis. Patients will be evaluated in terms of pain levels, functional\u002Fsymptom status, hand-finger strength, pressure pain threshold (PPT), tendon cross-sectional area measured by ultrasound, and the presence of effusion findings (semiquantitative; 0-3), and patient satisfaction.",[27,28,29,30,31],"Splints","Exercise Therapy","De Quervains Tenosynovitis","Pain Management","Ultrasonographic",[33,29,34,35,31],"pain","exercise therapy","splints","RECRUITING","2026-03-21",{"date":39,"type":40},"2026-03-24","ACTUAL",{"date":42,"type":40},"2025-05-29",{"date":44,"type":21},"2026-04-30",{"name":46,"class":47},"Konya Beyhekim Training and Research Hospital","OTHER_GOV",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":48},"100580511","ultrasonographic-analysis-of-post-traumatic-shoulder-lesions-after-hand-trauma-100580511","NCT06838247","Ultrasonographic Analysis of Post-Traumatic Shoulder Lesions After Hand Trauma","Detection of Simultaneous Presence of Shoulder Lesions in Patients With Hand Injuries by Diagnostic Ultrasonography","Inclusion Criteria:\n\n* Having a history of hand injury and applying for hand rehabilitation after surgical and conservative treatment.\n\nExclusion Criteria:\n\n* Being under 18 and over 65 years of age\n* Patients with systemic diseases (Diabetes mellitus, Peripheral vascular diseases)\n* Any rheumatic disease involving the hand and upper extremity\n* History of neuropathy involving the hand and upper extremity\n* Those with any shoulder problems prior to the hand injury\n* Those with an open wound on the hand\n* Those who cannot cooperate\n* Other upper extremity traumatic injuries occurring during the hand injury",{"count":57,"type":21},60,"OBSERVATIONAL","The purpose of the study is to reveal whether there are concurrent shoulder lesions in patients with hand injuries. Its importance is that it will shed light on whether not only the hand but also the shoulder should be included in the treatment program in hand rehabilitation.",[61,31,62],"Shoulder","Hand Injuries",[64,61,65,66],"Hand injuries","Diagnostic","Ultrasonography","2026-03-19",{"date":69,"type":40},"2026-03-23",{"date":71,"type":40},"2024-11-11",{"date":73,"type":21},"2026-07-01",{"name":75,"class":76},"Ankara Training and Research Hospital","OTHER",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":84,"sex":16,"minAge":17,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":88,"conditions":89,"keywords":92,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":48},"100628987","masseter-muscle-thickness-in-individuals-with-chronic-neck-pain-100628987","NCT07468786","Masseter Muscle Thickness in Individuals With Chronic Neck Pain","Comparison of Masseter Muscle Thickness Measured by Ultrasonography in Individuals With Chronic Neck Pain Compared to Healthy Individuals","Inclusion Criteria:\n\n* Be between the ages of 18 and 45\n* Have neck pain that has persisted for at least 3 months\n* Agree to participate in the study voluntarily and provide written informed consent\n\nExclusion Criteria:\n\n* History of cervical spine surgery or severe trauma\n* Diagnosis of cervical radiculopathy, myelopathy, or neurological disease\n* Rheumatic, inflammatory, or systemic musculoskeletal diseases\n* Diagnosed temporomandibular joint disorder (TMD)\n* Diagnosis of bruxism or a pronounced habit of teeth clenching\u002Fgrinding\n* History of manual therapy, injection, or surgical intervention in the face, jaw, or neck region within the last 6 months\n* Currently undergoing orthodontic treatment or history of orthodontic treatment within the last 6 months\n* Cognitive impairment or conditions that prevent understanding and responding to questionnaires",true,"45 Years",{"count":87,"type":21},90,"The primary objective of our study is to compare the thickness of the masseter muscle, measured by ultrasound, in individuals with chronic neck pain to that of healthy individuals. The secondary objective of the study is to examine the relationships between masseter muscle thickness and pain intensity, neck disability level, pain catastrophizing level, and clinical diagnostic criteria in individuals with chronic neck pain.",[90,31,91],"Masseter Muscle","Chronic Neck Pain",[93,94,95],"chronic neck pain","Ultrasonographic measurement","Masseter muscle","NOT_YET_RECRUITING","2026-03-09",{"date":99,"type":40},"2026-03-13",{"date":101,"type":21},"2026-03-20",{"date":103,"type":21},"2026-05-20",{"name":105,"class":76},"Hasan Kalyoncu University",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":84,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":113,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":114,"conditions":115,"keywords":118,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":48},"100625646","ultrasound-examination-of-the-vmo-in-patellofemoral-pain-syndrome-100625646","NCT07425340","Ultrasound Examination of the VMO in Patellofemoral Pain Syndrome","Ultrasonography Examination of the Vastus Medialis Obliquus and Vastus Medialis Longus Muscles in Patellofemoral Pain Syndrome","Inclusion Criteria:\n\n* Between the ages of 18 and 65\n* Have had localized pain in the front of the knee for at least the past 3 months\n* Experience pain during activities that require stair climbing, squatting, prolonged sitting, or knee flexion\n* Have been diagnosed with patellofemoral pain syndrome based on clinical evaluation\n* Volunteer to participate in the study and sign the informed consent form\n\nExclusion Criteria:\n\n* History of previous surgery on the knee joint\n* History of significant trauma to the knee region within the last 6 months\n* Diagnosis of meniscus, ligament injuries, knee osteoarthritis, or inflammatory rheumatic disease\n* Neurological diseases or systemic diseases affecting the musculoskeletal system\n* Presence of other lower extremity pathologies causing pain at a level that could affect measurements",{"count":20,"type":21},"The aim of this study is to examine in detail the ultrasonographic characteristics of the vastus medialis obliquus and vastus medialis longus muscles in individuals with patellofemoral pain syndrome and to compare these findings with those of healthy individuals. It is anticipated that the results obtained will contribute to a better understanding of the muscle-based mechanisms of PFAS and provide a scientific basis for the development of muscle-specific assessment and intervention strategies in physical therapy and rehabilitation practices.",[116,31,117],"Vastus Medialis","Patello Femoral Pain Syndrome",[119,120,94],"Patellofemoral Pain","Vastus Medialis Obliqus","2026-02-13",{"date":123,"type":40},"2026-02-20",{"date":125,"type":21},"2026-02-25",{"date":127,"type":21},"2026-06-25",{"name":105,"class":76},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":136,"targetDuration":4,"studyType":22,"phases":138,"briefSummary":139,"conditions":140,"keywords":144,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":4},"100617179","combined-ultrasonographic-skin-to-epiglottis-distance-with-modified-mallampati-versus-modified-mallampati-score-alone-in-predicting-difficult-laryngoscopy-during-tracheal-intubation-under-general-anesthesia-100617179","NCT07315256","Combined Ultrasonographic Skin-to-Epiglottis Distance With Modified Mallampati Versus Modified Mallampati Score Alone in Predicting Difficult Laryngoscopy During Tracheal Intubation Under General Anesthesia","Combined Ultrasonographic Skin-to-Epiglottis Distance With Modified Mallampati Versus Modified Mallampati Score Alone in Predicting Difficult Laryngoscopy During Tracheal Intubation Under General Anesthesia: A Prospective, Randomized Double Blinded Controlled Study","Inclusion Criteria:\n\n* Adults aged 18-65 years.\n* ASA physical status I-II.\n* Scheduled for elective surgery under general anesthesia requiring tracheal intubation with direct laryngoscopy.\n* Able to provide written informed consent.\n\nExclusion Criteria:\n\n* Emergency surgery.\n* Known or suspected difficult airway requiring planned alternative intubation technique (e.g., awake fiberoptic).\n* History of significant upper airway pathology, neck mass, prior neck surgery, or radiation affecting airway anatomy.\n* Limited mouth opening, cervical spine instability, or contraindication to standard sniffing position.\n* Pregnancy.\n* Refusal or inability to provide informed consent.",{"count":137,"type":21},160,[24],"This study will evaluate how well an ultrasound measurement of the distance from the skin to the epiglottis, when combined with the modified Mallampati score, can predict difficult laryngoscopy in adult patients undergoing elective surgery under general anesthesia. Adult patients scheduled for surgery requiring tracheal intubation will be randomly assigned to two assessment strategies before anesthesia: one group will have the usual bedside airway assessment with modified Mallampati alone, and the other group will have modified Mallampati plus a quick, painless ultrasound scan of the front of the neck to measure the skin-to-epiglottis distance. During intubation, the anesthesiologist, who is blinded to the preoperative assessments, will grade the laryngoscopic view using the Cormack-Lehane classification, and the investigators will compare how accurately each assessment approach predicts difficult laryngoscopy (grade 3-4). The study does not change how anesthesia or airway management is performed; ultrasound and clinical assessments are added solely for measurement and data collection, with minimal risk to participants and potential future benefits in improving airway risk stratification and patient safety.",[31,141,142,143],"Mallampati Score","Mallampati Score, Difficult Intubation, Videolaryngoscope","Tracheal Intubation",[145,143,146],"Difficult Laryngoscopy","Modified Mallampati","2025-12-18",{"date":149,"type":40},"2026-01-02",{"date":151,"type":21},"2026-01",{"date":153,"type":21},"2027-02",{"name":155,"class":76},"Assiut University",{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":11,"sex":16,"minAge":163,"maxAge":164,"enrollmentInfo":165,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":167,"conditions":168,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":173,"startDateStruct":175,"completionDateStruct":176,"leadSponsor":178,"locationsCount":48},"100567417","ultrasonographic-airway-assessment-in-predicting-difficult-laryngoscopy-in-pediatric-patients-undergoing-elective-surgery-100567417","NCT06667921","Ultrasonographic Airway Assessment in Predicting Difficult Laryngoscopy in Pediatric Patients Undergoing Elective Surgery","The Diagnostic Efficacy of Ultrasonographic Airway Assessment in Predicting Difficult Laryngoscopy in Pediatric Patients Undergoing Elective Surgery; A Prospective Observational Study","Inclusion Criteria:\n\n* Children aged (2-5) years old.\n* Both sexes.\n* American Society of Anesthesiology (ASA) physical status I or II.\n* Undergoing elective surgery under general anaesthesia with endotracheal intubation.\n\nExclusion Criteria:\n\n* Maxillofacial trauma\n* Large mass.\n* Scar under the chin.\n* History of neck surgery or congenital anomalies of the head and neck as difficult intubation is expected in these cases.","2 Years","5 Years",{"count":166,"type":21},308,"This study aims to evaluate the diagnostic accuracy of ultrasonographic airway examination in predicting difficult laryngoscopy in pediatric patients undergoing elective surgery.",[31,169,145,170,171],"Airway","Pediatric","Elective Surgery","2024-10-31",{"date":174,"type":40},"2024-11-01",{"date":172,"type":40},{"date":177,"type":21},"2025-09-01",{"name":179,"class":76},"Tanta University"]