[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644074":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":24,"centralContacts":29,"locations":10,"responsibleParty":34,"collaborators":10,"id":37,"slug":38,"hasResults":39,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":43,"eligibilityCriteria":44,"healthyVolunteers":39,"sex":45,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":10,"studyType":51,"phases":10,"briefSummary":52,"conditions":53,"keywords":10,"overallStatus":55,"whyStopped":10,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":10},{"fullName":5,"class":6},"Medipol University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients With Central Sensitization",null,"Patients with a preoperative Central Sensitization Inventory score of ≥40.",[13],"Procedure: Arthroscopic Rotator Cuff Repair",{"label":15,"type":10,"description":16,"interventionNames":17},"Patients Without Central Sensitization","Patients with a preoperative Central Sensitization Inventory score of \\\u003C40.",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"PROCEDURE","Arthroscopic Rotator Cuff Repair","All enrolled patients will undergo standard arthroscopic rotator cuff repair according to institutional clinical practice. The study is observational, and no additional intervention will be administered as part of the research protocol.",[9,15],[25],{"name":26,"affiliation":27,"role":28},"Erdal Güngör, M.D","Istanbul Medipol University, Department of Orthopedics and Traumatology","PRINCIPAL_INVESTIGATOR",[30],{"name":26,"role":31,"phone":32,"phoneExt":10,"email":33},"CONTACT","+905438790630","egungor_49@hotmail.com",{"type":28,"investigatorFullName":35,"investigatorTitle":36,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Erdal Güngör","Investigator Official Title:","100644074","preoperative-central-sensitization-and-postoperative-outcomes-after-arthroscopic-rotator-cuff-repair-100644074",false,"NCT07667257","Preoperative Central Sensitization and Postoperative Outcomes After Arthroscopic Rotator Cuff Repair","Effect of Central Sensitization on Postoperative Clinical Outcomes in Patients Undergoing Arthroscopic Rotator Cuff Repair","ARCS","Inclusion Criteria:\n\n* Inclusion Criteria:\n* Age between 18 and 65 years\n* Diagnosis of rotator cuff tear confirmed by clinical examination and magnetic resonance imaging (MRI)\n* Scheduled to undergo arthroscopic rotator cuff repair\n* Ability to understand and complete study questionnaires\n* Willingness to participate and provide informed consent\n\nExclusion Criteria:\n\n* Previous surgery on the affected shoulder.\n* Concomitant shoulder disorders requiring additional surgical procedures (e.g., fracture, instability, advanced glenohumeral osteoarthritis).\n* History of inflammatory rheumatic disease, active infection, or malignancy affecting the shoulder.\n* Neurological disorders that may influence pain perception or upper extremity function.\n* Severe psychiatric illness or cognitive impairment preventing completion of the questionnaires.\n* Pregnancy.\n* Inability or unwillingness to provide written informed consent.\n* Inability to attend the postoperative 3-month follow-up evaluation.","ALL","18 Years","65 Years",{"count":49,"type":50},50,"ESTIMATED","OBSERVATIONAL","This prospective observational study aims to investigate the effect of preoperative central sensitization on postoperative clinical outcomes in patients undergoing arthroscopic rotator cuff repair. Central sensitization, characterized by an increased responsiveness of the central nervous system to pain stimuli, has been associated with persistent pain and poor functional recovery in various musculoskeletal disorders. However, its impact on outcomes following arthroscopic rotator cuff repair has not been fully elucidated.\n\nAdult patients diagnosed with a rotator cuff tear by clinical examination and magnetic resonance imaging (MRI) and scheduled for arthroscopic repair will be enrolled. Preoperative central sensitization will be assessed using the Central Sensitization Inventory (CSI), while pain intensity and shoulder function will be evaluated using the Visual Analog Scale (VAS) and the Shoulder Pain and Disability Index (SPADI), respectively. Clinical assessments will be performed preoperatively and at postoperative 3 months. The study aims to determine whether preoperative central sensitization is associated with postoperative pain and functional recovery after arthroscopic rotator cuff repair.",[54],"Rotator Cuff Tear","NOT_YET_RECRUITING","2026-06-20",{"date":58,"type":59},"2026-06-25","ACTUAL",{"date":61,"type":50},"2026-06-30",{"date":63,"type":50},"2026-12-30",{"name":5,"class":6}]