VU University Medical Center
Amsterdam, North Holland, 1081, Netherlands
NCT Number: NCT01787903
The purpose of this study is to determine what the effects are of real-time continuous glucose monitoring on glycemia and quality of life in patients with type 1 diabetes mellitus and impaired hypoglycemia awareness.
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Notify Me18 year–70 year
All sexes
Interventional
Not applicable
Amsterdam, North Holland, 1081, Netherlands
The investigators hypothesize that the use of RT-CGM, relative to a control intervention using masked CGM, will result in improvement of various measures of glycemia and indicators of quality of life, reduce the occurrence of hypoglycemia and hyperglycemia and restore hypoglycemia awareness in T1DM patients with IHA. We will test this hypothesis by addressing the following research questions:
What is the effect of 16 weeks of RT-CGM use, versus 16 weeks of CGM use, in patients with T1DM and IHA on
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Active Comparator: MiniMed Paradigm® Veo™-system Placebo Comparator: iPro™2 Continuous Glucose Monitor (masked)
Other names: MiniMed Paradigm® Veo™-system, iPro™2 Continuous Glucose Monitor
Time frame: 45 weeks
The mean difference in time spent in the euglycemic range (interstitial glucose >3.9-<10.0 mmol/L), expressed as hours/day between the two 16-week intervention periods, i.e. RT-CGM versus masked CGM in patients with T1DM and IHA.
Time frame: 45 weeks
(diabetes-specific) markers of QoL, covering diabetes-related emotional distress (PAID-5), fear of hypoglycemia (HFS-2), self-efficacy (CIDS), health status (EQ5D) and emotional well-being (WHO-5)
Time frame: 45 weeks
Other glycemia variables, including HbA1c and time spent in hypo- and hyperglycemia ranges
Time frame: 45 weeks
The incidence and duration of hypoglycemic episodes
Time frame: 45 weeks
Changes in hypoglycemia awareness score according to Gold et al.
Time frame: 45 weeks
RT-CGM derived measures of glucose variability, e.g. SD, MODD, CONGA
Time frame: 45 weeks
The autonomic nervous system balance
Time frame: 45 weeks
The duration of wear of the RT-CGM device
Time frame: 45 weeks
The therapy adjustments made by patients during the interventions
Time frame: 45 weeks
Hypoglycemia awareness scores according to Clarke et al.
Time frame: 45 weeks
Satisfaction with use of CGM
Amsterdam UMC, location VUmc
Other
The Effects of Real-time Continuous Glucose Monitoring on Glycemia and Quality of Life in Patients With Type 1 Diabetes Mellitus and Impaired Hypoglycemia Awareness
Acronym: INCONTROL
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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