[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Ceragem Clinical Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":67},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100627242","electric-stimulation-home-usecgm-mepc2401-for-improving-blood-circulation-100627242",false,"NCT07446088","Electric Stimulation Home Use(CGM MEPC_2401) for Improving Blood Circulation","A Single-center, Open-label, Exploratory Clinical Trial to Evaluate the Safety and Efficacy of a Statics Electricity Generator for Electric Stimulation Home Use(CGM MEPC_2401) for Improving Blood Circulation","Inclusion Criteria:\n\n* Adults aged between 19 and 65 years\n* Individuals with a BMI of 30.0 kg\u002Fm² or less\n* Individuals without abnormal findings on hematology tests (CBC)\n\nExclusion Criteria:\n\n* Patients with uncontrolled hypertension despite medication (defined as systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥100 mmHg measured at rest)\n* Patients with medical conditions requiring the use of assistive devices (e.g., pacemaker, artificial joint, stent, prosthesis, etc.)\n* Patients with seizure disorders or a history of loss of consciousness (e.g., epilepsy, acute febrile convulsions such as those associated with severe fever, etc.), or those at high risk of electric shock due to such conditions\n* Patients with ventricular arrhythmias (e.g., ventricular tachycardia, history of coronary artery bypass surgery, etc.) and patients with neurological disorders (e.g., diabetic neuropathy, etc.)",true,"ALL","19 Years","65 Years",{"count":21,"type":22},40,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study is a single-center, open-label, exploratory clinical trial to evaluate the safety and efficacy of a statics electricity generator for improving blood circulation.",[28,29],"Improving Blood Circulation","Blood Circulation",[31],"blood circulation","RECRUITING","2026-02-25",{"date":35,"type":36},"2026-03-03","ACTUAL",{"date":38,"type":36},"2025-12-01",{"date":40,"type":22},"2026-06-30",{"name":42,"class":43},"Ceragem Clinical Inc.","INDUSTRY",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":18,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":23,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":44},"100626845","stress-urinary-incontinence-for-female-patients-cgm-muit-2301-100626845","NCT07440927","Stress Urinary Incontinence for Female Patients (CGM MUIT-2301)","A Multi-center, Prospective, Randomized, Double-blind, Sham Device Controlled Clinical Trial to Compare and Evaluate the Efficacy and Safety of the Use an Investigational Device (Model Name CGM MUIT-2301) and Sham Device (Model Name CGM MUIT-2301C) for Female Patients With Stress Urinary Incontinence","Inclusion Criteria:\n\n* Patients with urine leakage of ≥1 g on the standardized pad test\n\nExclusion Criteria:\n\n* Patients with mixed urinary incontinence with predominant urgency urinary incontinence\n* Patients with stress urinary incontinence\n* Patients with overflow urinary incontinence","FEMALE",{"count":54,"type":22},96,[25],"This study is a multicenter, prospective, randomized, double-blind, sham-controlled clinical trial conducted in female patients with stress urinary incontinence.",[58],"Stress Urinary Incontinence (SUI)",[58],{"date":61,"type":36},"2026-02-27",{"date":63,"type":36},"2024-12-13",{"date":65,"type":22},"2026-09-30",{"name":42,"class":43},""]