[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100328485":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":20,"locations":21,"responsibleParty":45,"collaborators":20,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":20,"eligibilityCriteria":52,"healthyVolunteers":49,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":20,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":20,"overallStatus":65,"whyStopped":20,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},{"fullName":5,"class":6},"Bayer","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients with knee pain","EXPERIMENTAL","Adults patients suffering from osteoarthritis pain or general knee pain",[13],"Device: BPI 1000013 (Dr Scholls Insole)",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","BPI 1000013 (Dr Scholls Insole)","Full length foam insole",[9],null,[22,35],{"facility":23,"status":20,"city":24,"state":25,"zip":26,"country":27,"countryCode":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":20},"Focus & Testing, Inc.","Calabasas","California","91302","United States","US",{"type":30,"coordinates":31},"Point",[32,33],-118.63842,34.15778,{"lat":33,"lon":32},{"facility":36,"status":20,"city":37,"state":38,"zip":39,"country":27,"countryCode":28,"cosmosGeoPoint":40,"geoPoint":44,"contacts":20},"The Wolf Group","Cincinnati","Ohio","45242",{"type":30,"coordinates":41},[42,43],-84.51439,39.12711,{"lat":43,"lon":42},{"type":46,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100328485","an-evaluation-of-a-gender-specific-insole-to-provide-relief-from-knee-pain-due-to-osteoarthritis-or-general-anterior-knee-pain-in-male-subjects-when-used-in-foot-wear-over-a-period-of-four-weeks-100328485",false,"NCT03556787","An Evaluation of a Gender Specific Insole to Provide Relief From Knee Pain Due to Osteoarthritis or General Anterior Knee Pain in Male Subjects When Used in Foot Wear Over a Period of Four Weeks","Inclusion Criteria:\n\n* Male subjects with age 18 to 70 years and a self-reported foot size between 8 and 14\n* Subjects with regular knee pain\n* Subjects with a baseline pain level of pain of ≥20 mm to ≤90 mm on 100 mm VAS scale at baseline (Visit 1)\n* Subjects must be able to walk unaided by cane or walker.\n\nExclusion Criteria:\n\n* Subjects with knee pain which is due to a recent injury","MALE","18 Years","70 Years",{"count":57,"type":58},89,"ACTUAL","INTERVENTIONAL",[61],"NA","The primary objective of this trial is to demonstrate the ability of a full length foam insole to provide relief from pain due to osteoarthritis of the knee or general knee pain when used in foot wear for a 4-week period of time.\n\nThe secondary objectives comprise the evaluation of the insole's ability to provide appropriate shoe fit and comfort as well as relief from osteoarthritis\u002F general knee pain after short-term use. The safety and tolerability of the test articles in terms of adverse events (AE) will also be investigated.",[64],"Osteoarthritis, Knee","COMPLETED","2018-11-20",{"date":68,"type":58},"2018-11-23",{"date":70,"type":58},"2018-06-04",{"date":72,"type":58},"2018-11-08",{"name":5,"class":6},2]