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Completed

NCT Number: NCT01787903

The Effects of RT-CGM on Glycemia and QoL in Patients With T1DM and IHA

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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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

VU University Medical Center

Amsterdam, North Holland, 1081, Netherlands

About this study

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

  • (primary objective:) time spent in euglycemia
  • (secondary objectives:)
  • (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)
  • other glycemia variables, including HbA1c and time spent in hypo- and - hyperglycemia ranges
  • the incidence and duration of hypoglycemic episodes
  • changes in hypoglycemia awareness score according to Gold et al.,
  • (tertiary objectives:)
  • measures of glucose variability
  • the autonomic nervous system balance
  • the duration of wear of the RT-CGM device
  • patients' therapy adjustments during the interventions
  • hypoglycemia awareness scores according to Clarke et al.
  • satisfaction with use of CGM
  • the number of contact moments not planned according to the study schedule
  • absence of work of patient (and spouse)
  • the global estimated costs of use of health care

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • T1DM, diagnosed according to ADA criteria regardless duration
  • Use of multiple daily injections of insulin (with a basal insulin injection and bolus injections) or continuous subcutaneous insulin infusion
  • Any HbA1c
  • Age between 18 and 70 years old (inclusive)
  • IHA according to the questionnaire by Gold et al.
  • Performing at least 3 SMBG/day or 21 SMBG/week

Exclusion criteria

  • Type 2 diabetes mellitus
  • History of (recent) major renal, liver, or (ischemic) heart disease (including cardiac conduction disorders)
  • Current untreated proliferative diabetic retinopathy
  • Current (treatment for) malignancy
  • Current use of non-selective beta-blockers
  • Current psychiatric disorders, including schizophrenia, bipolar disorder, anorexia nervosa or bulimia nervosa
  • Substance abuse or alcohol abuse (men >21 units/week, women >14 units/week)
  • Current pregnancy or intention to conceive
  • Current use of RT-CGM other than for short term (i.e. diagnostic use or use shorter than 3 consecutive months)
  • Hearing or vision impairment hindering perceiving of glucose display and alarms, or otherwise incapable of using a (RT-)CGM, in the opinion of the investigator
  • Poor commandment of the Dutch language or any (mental) disorder that precludes full understanding of the purpose and instructions of the study
  • Participation in another clinical study
  • Known or suspected allergy to trial product or related products

Treatment and study plan

Real-time continuous glucose monitor

Device

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

Primary outcomes

  1. Time spent in the euglycemic range

    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.

Secondary outcomes

  1. Quality of life

    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)

  2. Glycemia variables

    Time frame: 45 weeks

    Other glycemia variables, including HbA1c and time spent in hypo- and hyperglycemia ranges

  3. Hypoglycemic episodes

    Time frame: 45 weeks

    The incidence and duration of hypoglycemic episodes

  4. Changes in hypoglycemia awareness score

    Time frame: 45 weeks

    Changes in hypoglycemia awareness score according to Gold et al.

Other outcomes

  1. Glucose variability

    Time frame: 45 weeks

    RT-CGM derived measures of glucose variability, e.g. SD, MODD, CONGA

  2. ANS balance

    Time frame: 45 weeks

    The autonomic nervous system balance

  3. Sensor wear duration

    Time frame: 45 weeks

    The duration of wear of the RT-CGM device

  4. Therapy adjustments

    Time frame: 45 weeks

    The therapy adjustments made by patients during the interventions

  5. Hypoglycemia awareness score

    Time frame: 45 weeks

    Hypoglycemia awareness scores according to Clarke et al.

  6. RT-CGM satisfaction

    Time frame: 45 weeks

    Satisfaction with use of CGM

Sponsors and collaborators

Lead sponsor

Amsterdam UMC, location VUmc

Other

Collaborators

  • Eli Lilly and Company

Registry information

Official study title

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

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Feb 11, 2013
Registry last updated
Jul 26, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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