[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100573491":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":27,"locations":11,"responsibleParty":33,"collaborators":11,"id":35,"slug":36,"hasResults":37,"nctId":38,"briefTitle":39,"officialTitle":39,"acronym":11,"eligibilityCriteria":40,"healthyVolunteers":37,"sex":41,"minAge":42,"maxAge":11,"enrollmentInfo":43,"targetDuration":11,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":53,"overallStatus":56,"whyStopped":11,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":11},{"fullName":5,"class":6},"Mahidol University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Shockwave","EXPERIMENTAL",null,[13],"Device: Shockwave",{"label":15,"type":16,"description":11,"interventionNames":17},"Splint","ACTIVE_COMPARATOR",[18],"Device: Splint",[20,24],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":11},"DEVICE","In the Shockwave group, will be applied focused shockwaves therapy of 1500 impulses at 0.01 mJ\u002Fmm2 over the painful area or the pathologic flexor tendon to each participant under the supervision of a physiatrist. The ESWT will be conducted once weekly for 4 weeks with a sham splint (DIP joint blocking splints) for at least 8 hours per day for 6 weeks.",[9],{"type":21,"name":15,"description":25,"armGroupLabels":26,"otherNames":11},"In the splinting group, will be provided a PIP blocking splint at least 8 hours per day for 6 weeks with the sham shockwave (the patients close their eyes, extend their hand through a partition, apply shockwave device head with gel on the patient's finger, and play a mobile phone sound that mimics the sound of a real shockwave machine) once a week for 4 weeks.",[15],[28],{"name":29,"role":30,"phone":31,"phoneExt":11,"email":32},"Apisara Keesukphan, M.D., MS.c.,","CONTACT","6622011154","apisara.kee@mahidol.edu",{"type":34,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100573491","comparing-the-effects-of-extracorporeal-shockwave-therapy-and-splinting-in-the-treatment-of-trigger-finger-100573491",false,"NCT06746974","Comparing the Effects of Extracorporeal Shockwave Therapy and Splinting in the Treatment of Trigger Finger","Inclusion Criteria:\n\n* Patients age ≥ 18 years\n* Grade I-III trigger finger patients (patients who has the presence of tenderness over the A1 pulley or painful locking or triggering as they fixed and extended the finger)\n* Patients who consented to participation in the study\n\nExclusion Criteria:\n\n* Trigger thumb\n* The patients who had received previous treatment (steroid injection, ESWT or surgical release)\n* Patients with local infections, malignancies, severe coagulopathy and pregnancy","ALL","18 Years",{"count":44,"type":45},24,"ESTIMATED","INTERVENTIONAL",[48],"NA","The goal of this study is to compare the effects of extracorporeal shockwave therapy and splinting in the treatment of trigger finger.\n\nParticipants will:\n\nBe randomized into two groups (shockwave group and splint group). Visit the clinic once a week for four weeks for therapy. Keep a diary of their symptoms, which will be reviewed at six weeks.",[51,52],"Trigger Finger","Shockwave Therapy",[54,55],"trigger finger","shockwave","NOT_YET_RECRUITING","2024-12-18",{"date":59,"type":60},"2024-12-24","ACTUAL",{"date":62,"type":45},"2025-01-15",{"date":64,"type":45},"2026-11-30",{"name":5,"class":6}]