[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100647429":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":20,"locations":26,"responsibleParty":43,"collaborators":10,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":10,"eligibilityCriteria":50,"healthyVolunteers":47,"sex":51,"minAge":52,"maxAge":10,"enrollmentInfo":53,"targetDuration":10,"studyType":56,"phases":10,"briefSummary":57,"conditions":58,"keywords":10,"overallStatus":60,"whyStopped":10,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":70},{"fullName":5,"class":6},"Ohio State University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"SCS Trial Participants",null,"Participants undergoing a standard spinal cord stimulation (SCS) trial as part of routine clinical care will be observed. Daily pain scores, patient satisfaction, and decision-making regarding permanent SCS implantation will be collected during the trial period. No study-specific intervention will be administered; the study evaluates outcomes associated with the existing SCS trial process.",[13],"Procedure: Spinal Cord Stimulation (SCS) Trial",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"PROCEDURE","Spinal Cord Stimulation (SCS) Trial","This observational study will enroll approximately 42 subjects at The Ohio State University who are undergoing a spinal cord stimulation (SCS) trial as part of standard clinical care. No study-specific intervention will be assigned. Participants will be monitored to evaluate SCS trial outcomes, including pain scores, patient satisfaction, and decisions regarding permanent implantation. The sample size was selected to provide sufficient evaluable data while accounting for potential attrition and supporting descriptive and exploratory analyses.",[9],[21],{"name":22,"role":23,"phone":24,"phoneExt":10,"email":25},"Nasir Hussain, MD","CONTACT","6142933559","Nasir.Hussain@osumc.edu",[27],{"facility":28,"status":10,"city":29,"state":30,"zip":31,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"The Ohio State University","Columbus","Ohio","43210","United States","US",{"type":35,"coordinates":36},"Point",[37,38],-82.99879,39.96118,{"lat":38,"lon":37},[41],{"name":22,"role":23,"phone":42,"phoneExt":10,"email":25},"614-293-3559",{"type":44,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100647429","prospective-evaluation-of-the-optimal-scs-trial-length-100647429",false,"NCT07709351","Prospective Evaluation of the Optimal SCS Trial Length","Inclusion Criteria:\n\n1. Adults aged 18 years or older who are able to provide informed consent.\n2. Individuals with a clinical diagnosis of a chronic pain condition deemed appropriate for spinal cord stimulation (SCS) therapy by the treating physician.\n3. Individuals with a documented duration of chronic pain greater than 12 weeks.\n4. Individuals scheduled to undergo a spinal cord stimulation trial as part of routine clinical care at a participating site.\n\nExclusion Criteria:\n\n1. Pregnant individuals.\n2. Individuals currently receiving or involved in a worker's compensation claim related to their pain condition.\n3. Individuals with a history of a previously failed spinal cord stimulation (SCS) trial.\n4. Individuals with chronic opioid use exceeding 50 morphine milligram equivalents (MME) per day.","ALL","18 Years",{"count":54,"type":55},42,"ESTIMATED","OBSERVATIONAL","This study aims to determine the ideal length of a spinal cord stimulation (SCS) trial period by analyzing daily pain scores, patient satisfaction, and when patients decide whether to proceed with permanent implantation. The primary goal is to identify the shortest trial duration that can reliably predict SCS success. A secondary goal is to compare SCS trial outcomes with patient-reported health measures (PROMIS domains) and recommendations from the SCS E-Health Tool to evaluate how well these tools predict treatment candidacy and outcomes.",[59],"Spinal Cord Stimulation","NOT_YET_RECRUITING","2026-07-13",{"date":63,"type":64},"2026-07-16","ACTUAL",{"date":66,"type":55},"2026-08-28",{"date":68,"type":55},"2029-08-31",{"name":5,"class":6},1]