[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100484626":3},{"organization":4,"outcomesModule":7,"designInfo":24,"detailedDescription":23,"studyPopulation":23,"armGroups":30,"interventions":36,"overallOfficials":42,"centralContacts":23,"locations":46,"responsibleParty":66,"collaborators":23,"id":69,"slug":23,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":23,"eligibilityCriteria":74,"healthyVolunteers":70,"sex":75,"minAge":76,"maxAge":77,"enrollmentInfo":78,"targetDuration":23,"studyType":81,"phases":82,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":49,"whyStopped":23,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"Mayo Clinic","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":19,"otherOutcomes":23},[9,13,16],{"measure":10,"description":11,"timeFrame":12},"Change in pain","Measured using a visual analog scale (VAS), used to measure subjective pain, rated from 0 (no pain) to 100 (most severe pain) at rest and during activity (previously painful activities)","Baseline, 2, 6, 12 and 24-weeks post-procedure",{"measure":14,"description":15,"timeFrame":12},"Change in shoulder active range of motion","Measured using a goniometer reported in degrees",{"measure":17,"description":18,"timeFrame":12},"Change in shoulder strength","Assessed using a hand-held dynamometer (HHD) placed distally on the forearm, just proximal to the wrist joint along the distal radius and ulna with instruction to push into the HHD with maximum force production for approximately 5 seconds.",[20],{"measure":21,"description":22,"timeFrame":12},"Change in quality of life","Measured using the SF-36 Quality of Life questionnaire which is a 36-item self-reported health survey that measures health and disability. Possible scores range from 0 to 100, with 0 indicating maximum disability, and 100 indicating no disability.",null,{"allocation":25,"interventionModel":26,"interventionModelDescription":23,"primaryPurpose":27,"observationalModel":23,"timePerspective":23,"maskingInfo":28},"NA","SINGLE_GROUP","TREATMENT",{"masking":29,"maskingDescription":23,"whoMasked":23},"NONE",[31],{"label":32,"type":6,"description":33,"interventionNames":34},"Repair a partially torn rotator cuff","Subjects will undergo an ultrasonic tenotomy to repair a partially torn rotator cuff per standard of care as clinically indicated",[35],"Procedure: Ultrasonic tenotomy",[37],{"type":38,"name":39,"description":40,"armGroupLabels":41,"otherNames":23},"PROCEDURE","Ultrasonic tenotomy","Ultrasonic procedure as part of standard of care, as clinically indicated, to stimulate healing of the partial tear. The procedure uses ultrasound guidance that allows a needlelike device to gradually break up and remove tendinopathic tendon tissue.",[32],[43],{"name":44,"affiliation":5,"role":45},"Jacob Erickson, DO","PRINCIPAL_INVESTIGATOR",[47],{"facility":48,"status":49,"city":50,"state":51,"zip":52,"country":53,"countryCode":54,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Mayo Clinic Health System - Onalaska","RECRUITING","Onalaska","Wisconsin","54650","United States","US",{"type":56,"coordinates":57},"Point",[58,59],-91.23514,43.88441,{"lat":59,"lon":58},[62],{"name":44,"role":63,"phone":64,"phoneExt":23,"email":65},"CONTACT","608-392-9876","erickson.jacob@mayo.edu",{"type":45,"investigatorFullName":67,"investigatorTitle":68,"investigatorAffiliation":5,"oldNameTitle":23,"oldOrganization":23},"Jacob L. Erickson","Principal Investigator","100484626",false,"NCT05590494","Novel Treatment for Rotator Cuff Tears","Ultrasonic Tenotomy as a Treatment of Partial Rotator Cuff Tear of the Supraspinatus Tendon: A Pilot Feasibility Study","Inclusion Criteria:\n\n\\- Evidence of partial tear (\\\u003C 50%) of the supraspinatus tendon on MRI.\n\nExclusion Criteria:\n\n* A tear of the supraspinatus tendon greater \\> 50% and any areas of full thickness tearing, concomitant tears \\> 25% of other rotator cuff tendons (infraspinatus, teres minor or subscapularis), or acute tear of the glenoid labrum.\n* Evidence of systemic illness\u002Finfection requiring oral or IV antibiotics during the recruitment period.\n* Evidence of overlying skin infection or lesion at the proposed device insertion point on the shoulder.\n* Previous corticosteroid injection within three months.\n* Those individuals less than 25 and greater than 75 years of age will be excluded.","ALL","25 Years","75 Years",{"count":79,"type":80},15,"ESTIMATED","INTERVENTIONAL",[25],"The focus of this study is to examine changes in pain scores, strength, and range of motion over time following an ultrasonic tenotomy on a partial tear (\\\u003C50%) of the supraspinatus tendon of the rotator cuff.",[85],"Supraspinatus Tear",[39],"2025-07-29",{"date":89,"type":90},"2025-08-01","ACTUAL",{"date":92,"type":90},"2022-11-07",{"date":94,"type":80},"2028-12",{"name":5,"class":6},1]