[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100503594":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":32,"centralContacts":36,"locations":44,"responsibleParty":69,"collaborators":31,"id":71,"slug":72,"hasResults":73,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":31,"eligibilityCriteria":77,"healthyVolunteers":73,"sex":78,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":31,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":31,"overallStatus":60,"whyStopped":31,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"Cedars-Sinai Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental Group with Cortisone Injection of affected digit(s) and nighttime orthosis","EXPERIMENTAL","The experimental group will consist of receiving a PIP joint on the day they receive their cortisone injection. The Oval-8 ® will be issued to the subject by an Occupational Therapist to ensure correct fit and comfort as well as given written instructions for night use. The orthosis will be worn at night for 6-week duration. Participants will have 1 follow up phone call or email at the 6-week mark and then 1 follow up phone call or email at the 12 week mark by a member of the research team from the time they received their cortisone injection where the time for resolution of trigger finger symptoms, VAS (Visual Analogue Scale), subjective questionnaire and QuickDASH scores will all be recorded in their medical research file.",[13],"Device: Oval-8 ® Orthosis",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group-No Orthosis","ACTIVE_COMPARATOR","The control group will be identical to the experimental group except without the use of a nighttime orthosis. Participants will have 1 follow up phone call or email at the 6-week mark and then 1 follow up phone call or email at the 12 week mark by a member of the research team from the time they received their cortisone injection where the time for resolution of trigger finger symptoms, VAS (Visual Analogue Scale), subjective questionnaire and QuickDASH scores will all be recorded in their medical research file.",[19],"Other: Cortisone injection only",[21,27],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"DEVICE","Oval-8 ® Orthosis",[9],[26],"Cortisone Injection",{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"Cortisone injection only","The control group will receive a cortisone injection and be instructed to move their fingers normally",[15],null,[33],{"name":34,"affiliation":5,"role":35},"Meghan McCullough, MD","PRINCIPAL_INVESTIGATOR",[37,42],{"name":38,"role":39,"phone":40,"phoneExt":31,"email":41},"Theodore Brown, BS","CONTACT","800-700-6424","Theodore.Brown@cshs.org",{"name":34,"role":39,"phone":31,"phoneExt":31,"email":43},"Meghan.McCullough@cshs.org",[45,59],{"facility":46,"status":47,"city":48,"state":49,"zip":50,"country":51,"countryCode":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":31},"Cedars-Sinai Medical Center Outpatient Rehabilitation Hand Clinic","COMPLETED","Los Angeles","California","90048","United States","US",{"type":54,"coordinates":55},"Point",[56,57],-118.24368,34.05223,{"lat":57,"lon":56},{"facility":5,"status":60,"city":48,"state":49,"zip":50,"country":51,"countryCode":52,"cosmosGeoPoint":61,"geoPoint":63,"contacts":64},"RECRUITING",{"type":54,"coordinates":62},[56,57],{"lat":57,"lon":56},[65],{"name":66,"role":39,"phone":67,"phoneExt":31,"email":68},"Theodore Brown","310-423-9200","theodore.brown@cshs.org",{"type":35,"investigatorFullName":34,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":31,"oldOrganization":31},"Physician","100503594","conservative-treatment-of-trigger-finger-100503594",false,"NCT05837286","Conservative Treatment of Trigger Finger","Conservative Treatment of Trigger Finger: Outcomes of a Randomized Controlled Trial","Inclusion Criteria:\n\n* Individuals 18 years old or older are included\n* Patients with trigger finger, aka stenosing flexor tenosynovitis\n* Status post receiving cortisone injection of the affected digit(s)\n\nExclusion Criteria:\n\n* Any records flagged with break the glass or research opt out\n* Patients with rheumatoid arthritis\n* Patients with a history of traumatic injury to the hand\n* Cognitive or behavioral problems which would preclude informed consent\n* Unable to speak and understand English","ALL","18 Years","100 Years",{"count":82,"type":83},146,"ESTIMATED","INTERVENTIONAL",[86],"NA","This study is to analyze the effectiveness of a nighttime extension orthosis after receiving a cortisone injection for the treatment of trigger finger to improve pain and restore functional outcomes. The investigators hypothesize that the extension orthosis will improve pain and functional outcomes compared to those without a digital night extension orthosis in those with trigger finger at 12 weeks from the injection.",[89,90],"Hand Injuries","Trigger Finger","2026-03-24",{"date":93,"type":94},"2026-03-27","ACTUAL",{"date":96,"type":94},"2023-08-01",{"date":98,"type":83},"2026-05-31",{"name":5,"class":6},2]