Drug Therapy Clinical Trial
Official title:
Comparison of the Efficacy of Sensor-augmented Pump Therapy Versus Hybrid Closed-loop Glucose Management (MiniMed670G™) in Patients With Type 1 Diabetes at Home in a Randomized Controlled Trial
Closed loop technology has been shown to reduce both hypoglycemia and hyperglycemia, as well as reduce glycemic variability. Sensor augmented pump (SAP) therapy means the addition of alerts according to high or low glucose values as well as trend arrows showing actual glucose trends to pump therapy. This Hybrid closed loop (HCL) system provides several additional effects compared to SAP therapy: according to actual and predicted sensor glucose values, the insulin therapy can be adopted automatically by pump: in case of high values (or predicted) more insulin will be administered, in case of low values (or predicted) the insulin infusion will be decreased a suspended and resumed again. So the HCL provides a lot more automatic functions to keep glucose in target compared to SAP. The aim of the current trial is to compare the SAP-therapy with the hybrid closed loop glucose management in patients with type 1 diabetes at home.
Monocentric, randomized, controlled cross-over safety evaluation study. For the study, 20 subjects per age group (small children 2-<9 years, children/adolescents ≥9-14 years) will be enrolled (total n=40). The study is anticipated to last no longer than 6 months from investigational center initiation to completion of all data entry and monitoring procedures. It is estimated that all subjects will be enrolled into the study within approximately 3 months of study start. - Visit 1 - Day 0: (Subjects come to clinic): Consent, Screening (incl. blood sample) and device training, training to emergency behavior; Pump Start in low glucose suspend mode, alarm settings - Visit 2 - Week 1: Subjects come to clinic; start Run-in Period and start Sensor Augmented Pump (SAP) therapy without any SmartGuard feature, assessment of AEs; pump will be read out, data stored; subjects will be trained to use the Auto mode, Auto mode will be activated. All subjects will participate in a 11-week study period. - Visit 3 - Week 2: Subjects are randomized to start with SAP or Hybrid Closed Loop (HCL) therapy and stay with an assigned therapy for next 4 weeks. - Visit 4 - Week 6: End of Period 1 and start of washout period. Subjects stay in this period with SAP therapy only. Evaluation of past 4 weeks, assessment of AEs - Visit 5 - Week 7: Period 2 starts. Evaluation of past week, assessment of AEs. SAP group will be using 670G with HCL and HCL group will be using SAP therapy for next 4 weeks. - Visit 6 - Week 11: End of Study, Subjects come to clinic; evaluation of past 4 weeks, assessment of AEs, HbA1c; pump will be read out, data stored. All study material will be given back. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Enrolling by invitation |
NCT02588560 -
Viral Load Changes in Lymphoma Patients With HCV Infection After Chemotherapy
|
N/A | |
Completed |
NCT05366621 -
Post-fracture Medication and Mortality
|
||
Recruiting |
NCT03487939 -
Neoadjuvant FOLFOXIRI Chemotherapy in Resectable Liver Metastasis of Colorectal Cancer
|
Phase 2 | |
Recruiting |
NCT04478838 -
"Extended" (Alternate Day) Antipsychotic Dosing
|
Phase 4 | |
Recruiting |
NCT05322967 -
Effect of Chronotherapy on Blood Pressure - Time of Intake of Blood Pressure Lowering Drugs
|
N/A | |
Not yet recruiting |
NCT01131429 -
A Chinese Randomized Crossover Study of Erlotinib Versus Docetaxel/Cisplatin in Previously Untreated Stage IIIB/IV Lung Adenocarcinoma With EGFR Mutations
|
Phase 2 | |
Recruiting |
NCT06223568 -
Phase II Trial of Neoadjuvant Chemotherapy (NAC) Alone or in Combination With Immunotherapy Vaccine PRGN-2009 in Subjects With Newly Diagnosed HPV-Associated Oropharyngeal (Head and Neck) Cancer
|
Phase 2 | |
Completed |
NCT04627077 -
Livestrong Cancer Institutes' Patient Reported Outcomes Study
|
||
Recruiting |
NCT06009965 -
Efficacy of IST Combined With TPO-RA in the Treatment of AA and Establishment of a Recurrence Prediction System
|
Phase 4 | |
Completed |
NCT03551457 -
Potential Therapeutic Response In Urogenital Tumors
|
||
Completed |
NCT04095104 -
Adjunct Phentermine + Topiramate After Bariatric Surgery in 12-24 Year Olds
|
Phase 2 | |
Recruiting |
NCT04996732 -
Long-term Survivorship of Discharged Patients With Malignant Tumor Based on Single-institutional Cancer Registry
|
||
Not yet recruiting |
NCT05246722 -
Registry Study of Pharmacotherapy and Clinical Outcomes in Elderly Patients With Coronary Heart Disease (PHARM-ageing)
|
||
Completed |
NCT04141657 -
Safety Analysis of Antimicrobial Pharmacotherapy in Intensive Care Unit at Pediatric Hospital
|
||
Not yet recruiting |
NCT04184583 -
Registry Study on Drug Therapy and Clinical Outcomes in Patients With Acute Coronary Syndrome
|
||
Completed |
NCT04493905 -
Effects of Anesthetic Techniques on Time to Start of Adjuvant Chemotherapy Following Surgery for Colorectal Cancer
|
||
Completed |
NCT01199393 -
Genetic Polymorphisms Predict Chemotherapeutic Outcomes in Patients With Metastatic Breast Cancer
|
N/A | |
Recruiting |
NCT03484221 -
Totally Neoadjuvant FOLFOXIRI + Short-course Radiation + XELOX in Patients With Locally Advanced Rectal Cancer
|
Phase 2 | |
Recruiting |
NCT03484195 -
Neoadjuvant FOLFOXIRI Chemotherapy in Patients With Locally Advanced Colon Cancer
|
Phase 2 | |
Completed |
NCT00122122 -
Randomized Controlled Trial of Enhanced Pharmacy Care in Older Veteran Outpatients
|
Phase 3 |