[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100564172":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":32,"locations":26,"responsibleParty":38,"collaborators":26,"id":42,"slug":26,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":26,"eligibilityCriteria":47,"healthyVolunteers":43,"sex":48,"minAge":49,"maxAge":26,"enrollmentInfo":50,"targetDuration":26,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":26,"overallStatus":63,"whyStopped":26,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":26},{"fullName":5,"class":6},"New York Presbyterian Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","ACTIVE_COMPARATOR","Standard postoperative care for patients undergoing rotator cuff repair.",[13],"Procedure: Standard postoperative care",{"label":15,"type":16,"description":17,"interventionNames":18},"Sleep Aid Group","EXPERIMENTAL","Standard postoperative care for patients undergoing rotator cuff repair PLUS the use of the sleep assistive device postoperatively.",[13,19],"Device: Surgical Recovery Systems Sleep Aid",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Standard postoperative care","This will include medications, rehabilitation schedules, and follow-up visits as normally scheduled.",[9,15],null,{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":26},"DEVICE","Surgical Recovery Systems Sleep Aid","Sleep assistive device",[15],[33],{"name":34,"role":35,"phone":36,"phoneExt":26,"email":37},"Cole Morrissette, MD","CONTACT","3322153690","crm2224@cumc.columbia.edu",{"type":39,"investigatorFullName":40,"investigatorTitle":41,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Cole Morrissette","Resident Orthopedic Surgeon","100564172",false,"NCT06625723","Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery","Investigating the Impact of a Sleep Aid on Sleep and Recovery Following Rotator Cuff Repair Surgery","Inclusion Criteria:\n\n* Rotator Cuff Tear\n\nExclusion Criteria:\n\n* Prior ipsilateral shoulder surgery\n* Ipsilateral upper extremity neurological deficit","ALL","18 Years",{"count":51,"type":52},60,"ESTIMATED","INTERVENTIONAL",[55],"NA","Postoperative recovery following a rotator cuff repair surgery can be challenging. In particular, sleeping is difficult given the restrictions of the operative shoulder. This study aims to evaluate a postoperative sleep device that will allow for safe and comfortable positioning of the arm, with the anticipated effect to improve postoperative recovery and sleep.",[58,59,60,61,62],"Rotator Cuff Tears","Rotator Cuff Injuries","Shoulder Pain","Shoulder Injuries","Shoulder Impingement","NOT_YET_RECRUITING","2024-11-14",{"date":66,"type":67},"2024-11-18","ACTUAL",{"date":69,"type":52},"2024-12-01",{"date":71,"type":52},"2027-04-01",{"name":5,"class":6}]