[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635256":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":37,"responsibleParty":50,"collaborators":26,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":26,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":26,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":72,"overallStatus":78,"whyStopped":26,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"Haydarpasa Numune Training and Research Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Ultrasound-Guided Dry Needling","EXPERIMENTAL","Participants will receive ultrasound-guided dry needling applied to the common extensor tendon once weekly for five sessions. All participants will also perform a standardized home exercise program.",[13],"Procedure: Ultrasound-guided dry needling",{"label":15,"type":16,"description":17,"interventionNames":18},"Extracorporeal Shock Wave Therapy","ACTIVE_COMPARATOR","Participants will receive radial extracorporeal shock wave therapy applied to the lateral epicondyle once weekly for five sessions. All participants will also perform a standardized home exercise program.",[19],"Device: Extracorporeal Shock Wave Therapy",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Ultrasound-guided dry needling","Dry needling will be performed under ultrasound guidance targeting the tendinosis area of the common extensor tendon. The procedure will be applied once weekly for five sessions.",[9],null,{"type":28,"name":15,"description":29,"armGroupLabels":30,"otherNames":26},"DEVICE","Radial extracorporeal shock wave therapy will be applied using standard parameters (10-15 Hz, 1.5-2.5 bar, 2000 pulses) once weekly for five sessions.",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"Berna Gunay, MD","CONTACT","+90 535 413 3047","bernagunay@yahoo.com",[38],{"facility":5,"status":26,"city":39,"state":39,"zip":40,"country":41,"countryCode":26,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Istanbul","34662","Turkey (Türkiye)",{"type":43,"coordinates":44},"Point",[45,46],28.94966,41.01384,{"lat":46,"lon":45},[49],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},{"type":51,"investigatorFullName":33,"investigatorTitle":52,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Specialist in Physical Medicine and Rehabilitation","100635256","dry-needling-vs-eswt-in-lateral-epicondylitis-100635256",false,"NCT07550322","Dry Needling vs ESWT in Lateral Epicondylitis","Ultrasound-Guided Dry Needling Versus Extracorporeal Shock Wave Therapy in Lateral Epicondylitis: A Randomized Single-Blind Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18 to 65 years\n* Clinical diagnosis of lateral epicondylitis\n* Symptoms persisting for at least 6 weeks\n* Pain over the lateral epicondyle aggravated by wrist extension or gripping activities\n* Positive provocative tests consistent with lateral epicondylitis (e.g., Cozen's test and\u002For Mill's test)\n* Ability to understand the study procedures and provide written informed consent\n\nExclusion Criteria:\n\n* Previous surgery for lateral epicondylitis in the affected elbow\n* Corticosteroid injection, PRP injection, prolotherapy, mesotherapy, or ESWT to the affected elbow within the previous 6 months\n* Bilateral lateral epicondylitis requiring simultaneous treatment\n* Cervical radiculopathy or other neurologic disorders affecting the upper extremity\n* Inflammatory rheumatic disease\n* Elbow osteoarthritis or significant structural elbow pathology\n* Full-thickness tendon tear or other major tendon injury on imaging\n* Pregnancy or breastfeeding\n* Active infection, skin lesion, or wound at the treatment site\n* Use of anticoagulant therapy or bleeding disorder\n* Inability to comply with follow-up assessments","ALL","18 Years","65 Years",{"count":64,"type":65},60,"ESTIMATED","INTERVENTIONAL",[68],"NA","This randomized single-blind controlled trial aims to compare the effectiveness of ultrasound-guided dry needling and extracorporeal shock wave therapy in patients with lateral epicondylitis. Sixty participants aged 18-65 years will be randomized into two groups. The dry needling group will receive ultrasound-guided tendon fenestration once weekly for five sessions, while the ESWT group will receive radial extracorporeal shock wave therapy once weekly for five sessions. All participants will be given a standardized home exercise program. Pain, function, grip strength, pressure pain threshold, quality of life, and ultrasonographic findings will be evaluated at baseline, post-treatment, and at 3- and 6-month follow-up. The primary outcome is change in pain severity measured by Visual Analog Scale.",[71],"Lateral Epicondylitis (Tennis Elbow)",[73,74,23,75,76,77],"Lateral epicondylitis","Dry needling","Extracorporeal shock wave therapy","ESWT","Musculoskeletal ultrasound","NOT_YET_RECRUITING","2026-04-19",{"date":81,"type":82},"2026-04-24","ACTUAL",{"date":84,"type":65},"2026-05-01",{"date":86,"type":65},"2027-01-15",{"name":5,"class":6},1]