[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100603362":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":39,"responsibleParty":59,"collaborators":61,"id":65,"slug":66,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":24,"eligibilityCriteria":71,"healthyVolunteers":67,"sex":72,"minAge":73,"maxAge":74,"enrollmentInfo":75,"targetDuration":24,"studyType":78,"phases":79,"briefSummary":81,"conditions":82,"keywords":86,"overallStatus":42,"whyStopped":24,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"Tulane University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Self-Monitoring of Blood Glucose (SMBG)","PLACEBO_COMPARATOR","The study participants will be randomized to the self-monitoring group (control) after a period of two-week run-in and followed for 6 months. They will be given an opportunity to wear the CGM sensor for 3 months at the conclusion of the 6-month follow-up as an optional follow-up.",[13],"Device: Continuous Glucose Monitoring (CGM)",{"label":15,"type":16,"description":17,"interventionNames":18},"Continuous Glucose Monitoring (CGM)","ACTIVE_COMPARATOR","The study participants will be randomized to the continuous glucose monitoring group (intervention).",[13],[20],{"type":21,"name":15,"description":22,"armGroupLabels":23,"otherNames":24},"DEVICE","Continuous glucose monitors will be placed subcutaneously every 14 days.",[15,9],null,[26],{"name":27,"affiliation":5,"role":28},"Shaveta Gupta, MD","PRINCIPAL_INVESTIGATOR",[30,35],{"name":31,"role":32,"phone":33,"phoneExt":24,"email":34},"Neha Upadhyay, BDS,MPH","CONTACT","5049889803","nupadhyay@tulane.edu",{"name":36,"role":32,"phone":37,"phoneExt":24,"email":38},"Ayitevi Agbodji, MD,MPH&TM","504-988-9839","aagbodji@tulane.edu",[40],{"facility":41,"status":42,"city":43,"state":44,"zip":45,"country":46,"countryCode":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"University Medical Center","RECRUITING","New Orleans","Louisiana","70112","United States","US",{"type":49,"coordinates":50},"Point",[51,52],-90.07507,29.95465,{"lat":52,"lon":51},[55,57,58],{"name":31,"role":32,"phone":56,"phoneExt":24,"email":34},"504-988-9803",{"name":36,"role":32,"phone":37,"phoneExt":24,"email":38},{"name":27,"role":28,"phone":24,"phoneExt":24,"email":24},{"type":60,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR",[62],{"name":63,"class":64},"Abbott","INDUSTRY","100603362","continuous-glucose-monitoring-cgm-in-an-underserved-population-100603362",false,"NCT07135531","Continuous Glucose Monitoring (CGM) in an Underserved Population","Continuous Glucose Monitoring in an Underserved Population: Impact on Glucose Control, Patient Reported Outcomes, Healthcare Utilization, and Long Term Complications","Inclusion Criteria:\n\n* Age 18-75 years\n* Type 2 diabetes mellitus\n* HbA1C ≥ 7.5%\n* At least on 1 insulin injection therapy daily\n* Patients established with primary care clinic or endocrinology clinic or diabetes clinics in the New Orleans and surrounding areas\n* Patients with Medicaid or free care or uninsured\n* Patients must be able to speak and understand English and be capable of providing informed consent to participate in the study\n\nExclusion Criteria:\n\n* Type 1 diabetes mellitus\n* Currently on CGM or using insulin pump\n* Advanced renal disease or Estimated Glomerular Filtration Rate (eGFR) \\\u003C40\n* Serious co-morbidities which in the investigator's opinion, will make it challenging for patients to participate\n* The patient has been diagnosed with end-stage renal disease, is on dialysis, or has had a kidney transplant, Hemoglobinopathies, iron therapy or other condition that interferes with HbA1c measurement\n* Pregnant","ALL","18 Years","75 Years",{"count":76,"type":77},50,"ESTIMATED","INTERVENTIONAL",[80],"NA","The investigators aim is to conduct a randomized clinical trial in an underserved population who are either uninsured or on Medicaid and taking at least one injection of insulin daily. The investigators believe that this study will lead to considerable alleviation of health disparities and provide better care for an underserved population. This will be a pilot study to evaluate the feasibility of such a trial in this population before doing a larger multicenter trial.",[83,84,85],"Diabetes","Diabetes Mellitus","Diabetes Type 2",[87,88,89,90],"Medicaid","Underinsured","Continuous glucose monitoring","Uninsured","2026-05-03",{"date":93,"type":94},"2026-05-05","ACTUAL",{"date":96,"type":94},"2026-03-19",{"date":98,"type":77},"2027-07",{"name":5,"class":6},1]