[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"de-quervain-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:de-quervain-disease":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,43,82],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100538871","de-quervains-disease-in-the-acute-phasea-study-aimed-at-evaluating-the-effectiveness-of-standard-physiotherapy-treatment-handguide-compared-to-experimental-treatment-after-performing-ultrasound-guided-infiltrative-therapy-100538871",false,"NCT06296472","De Quervain's Disease in the Acute Phase:a Study Aimed at Evaluating the Effectiveness of Standard Physiotherapy Treatment (HANDGUIDE), Compared to Experimental Treatment After Performing Ultrasound-guided Infiltrative Therapy.","De Quervain's Disease in the Acute Phase: Randomized Interventional Study Aimed at Evaluating the Effectiveness of Standard Physiotherapy Treatment (HANDGUIDE), Compared to Experimental Treatment After Performing Ultrasound-guided Infiltrative Therapy.","Inclusion Criteria:\n\n* Patients of both sexes with a minimum age of 18 years;\n* Medical diagnosis of de Quervain syndrome assessed through orthopedic clinical examination e confirmation by ultrasound;\n* Signing of the informed consent and participation in the study.\n\nExclusion Criteria:\n\n* Patients who are not self-sufficient or not able to understand and want;\n* Presence of other pathologies in the hand affected by de Quervain pathology, such as intersection syndrome, neuropathies, fractures, rhizoarthrosis, arthrosis of the radio-carpal or intercarpal joint, intercarpal instability, cervical radiculopathy, rheumatic or metabolic pathologies;\n* Pregnant or breastfeeding women.","ALL","18 Years",{"count":19,"type":20},134,"ESTIMATED","INTERVENTIONAL",[23],"NA","The objective of the study is to compare pain reduction and disability reduction in two groups of patients diagnosed with de Quervain syndrome who will undergo ultrasound-guided infiltrative treatment with corticosteroid as per normal clinical practice:\n\n* the control group will subsequently be subjected to a standard treatment based on the European guidelines of the HANDGUIDE group,\n* the experimental group will subsequently carry out a program of eccentric exercises.",[26,27],"De Quervain Disease","Hand Tenosynovitis",[29],"Hand rehabilitation","RECRUITING","2026-04-28",{"date":33,"type":34},"2026-05-04","ACTUAL",{"date":36,"type":34},"2024-02-27",{"date":38,"type":20},"2026-12-30",{"name":40,"class":41},"Istituto Ortopedico Rizzoli","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":62,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":42},"100605159","understanding-patient-preferences-when-deciding-on-a-voluntary-musculoskeletal-test-100605159","NCT07158892","Understanding Patient Preferences When Deciding on a Voluntary Musculoskeletal Test","Confirmation of Values and Preferences When Considering a Musculoskeletal Diagnostic Test: A Scenario-Based Study","Inclusion Criteria:\n\n* Adults (18+ years)\n* English literacy\n* Seeking musculoskeletal specialty care\n* Diagnosis of non-traumatic musculoskeletal condition (including but not limited to: carpal tunnel syndrome, lateral epicondylitis, osteoarthritis, trigger digit, Dupuytren's, De Quervain, or rotator cuff tendinopathy)\n\nExclusion Criteria:\n\n* Cognitive or physical impairment or severe psychiatric illness that would interfere with participation in the scenario-based discussion or completion of the survey instruments",{"count":51,"type":20},220,[23],"The goal of this clinical trial is to understand how people make decisions about imaging tests for common musculoskeletal problems (like arthritis, tendon problems, or nerve compression). The study involves adult patients attending a musculoskeletal specialty clinic.\n\nThe main questions it aims to answer are:\n\n1. Does having a structured conversation about the pros and cons of a test affect how much a person wants to have that test?\n2. Does that conversation help people feel more confident and less conflicted about their decision?\n\nResearchers will compare patients who have a values-based discussion with a researcher to those who receive brief written information about the test, to see if these approaches affect how people feel about having the test.\n\nParticipants will:\n\n* Read a brief scenario about a proposed diagnostic imaging test (like an X-ray, MRI, CT, or ultrasound).\n* Either take part in a short structured conversation or read brief information about the test.\n* Answer a short survey about their thoughts on the test.\n\nThis study does not involve actual medical testing or affect your clinical care. It is for research purposes only.",[55,56,57,58,59,60,61,26],"Non-traumatic Musculoskeletal Conditions","Carpal Tunnel Syndrome (CTS)","Lateral Epicondylitis","Osteoarthritis","Trigger Digit","Dupuytren Contracture","Rotator Cuff Tendinopathy",[63,64,65,66,67,68,69,70,71],"Musculoskeletal disorders","Diagnostic imaging","Shared decision making","Advance care planning (ACP)","Patient preferences","Health communication","Decision conflict","Scenario-Based Study","Orthopedic care","NOT_YET_RECRUITING","2025-09-02",{"date":75,"type":34},"2025-09-08",{"date":77,"type":20},"2025-09-10",{"date":79,"type":20},"2026-03-01",{"name":81,"class":41},"University of Texas at Austin",{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":88,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":90,"enrollmentInfo":91,"targetDuration":4,"studyType":21,"phases":93,"briefSummary":95,"conditions":96,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":42},"100517019","phase-4-impact-of-gel-aromatherapy-on-pain-for-patients-with-de-quervain-disease-100517019","NCT06012097","Impact of Gel Aromatherapy on Pain for Patients With De Quervain Disease","Impact of Gel Aromatherapy on Pain for Patients With De Quervain Disease : Monocentric Study, Controlled, Randomized, Partially Blinded, in Paralleled Groups","Helping Hand","Inclusion Criteria:\n\n* Male or female patient aged 18 to 75,\n* Patient with unilateral De Quervain's tenosynovitis,\n* Patient cared in the Hand Surgery Department, SOS Mains Emergency Department or Rheumatology Department of Strasbourg University Hospitals,\n* Patient informed of the results of the prior medical examination,\n* Informed consent signed by the patient,\n* Patient affiliated to a health insurance social protection scheme or beneficiary,\n* For a woman of childbearing potential, negative urine pregnancy test at the inclusion visit and maintenance of effective contraception throughout the study.\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding patient,\n* Patient allergic to a component of the gel with essential oils, Dicloflenac®, NSAIDs, or one of the excipients\n* Patient treated with oral non-steroidal anti-inflammatory drugs\n* Patient with ongoing treatment with another ointment at the treatment application site (radial edge of the wrist)\n* Patient with damaged skin, whatever the lesion: oozing dermatosis, eczema, infected lesion, burn or wound,\n* Patient with atopic skin disease,\n* Patient with epilepsy or with a history of epilepsy,\n* Patient with a history of homolateral De Quervain's tenosynovitis, or having already had corticosteroid infiltrations in the 6 months before his inclusion on the ipsilateral side of the pathology,\n* Patient with associated tendinopathies in the elbow or forearm region,\n* Impossibility of giving the patient information (patient in an emergency situation, patient with difficulties of understandin, agitation of the patient),\n* Patient under legal protection, under guardianship or curatorship.","75 Years",{"count":92,"type":20},70,[94],"PHASE4","De Quervain disease is characterized by an adductor pollicis longus and extensor pollicis brevis tendons inflammation as thys pass beneath the extensor retinaculum at the radial styloid. This pathology is recognized as a musculoskeletal disorder of the upper limb triggering functional deficits resulting to possible modifications in the professional activity, sources of absenteeism, thus constituting an economic cost for society. At the etiological level, this pathology also affects young mothers (it's called \"mother's wrist\" or mommy thumb\"), mobile phone users (\"textonite\", \"Blackberryte\") or video game players (\"Nintendoite\").\n\nCurrently, the treatment is mainly conservative by splint and anti-inflammatory gel and\u002For corticosteroid infiltration. Howewer, these therapies have undesirable effects. The interest of this study is therefore to propose another therapy based on aromatherapy gel.",[26],"2025-08-01",{"date":99,"type":34},"2025-08-03",{"date":101,"type":34},"2024-06-04",{"date":103,"type":20},"2026-04-01",{"name":105,"class":41},"University Hospital, Strasbourg, France"]