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NCT04387422Active, not recruiting

Recurrent Hypoglycemia in Type 1 Diabetes (Aim 2)

Measurement of Glucose Homeostasis in Human Brain by NMR: Effect of Recurrent Hypoglycemia on Type 1 Diabetes (Aim 2)

Source: ClinicalTrials.gov · Last updated 8 Apr 2026

Brief summary (registry, in English)

This study will explore the cerebral mechanisms of impaired awareness of hypoglycemia (IAH) in type 1 diabetics following exposure to experimental recurrent hypoglycemia (HG). To induce IAH, patients with T1D identified to have normal awareness of hypoglycemia (NAH) will undergo three 2-hour long hypoglycemic clamps. Neurochemical profiles will be measured by high field MRS before and after induction of IAH. Subject glycemic variability and activity/sleep for 1 week before each study will be monitored as all factors have been shown to alter responses to HG.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
31 Jan 2020
Start date
12 Aug 2020
Primary completion date
Dec 2028
Lead sponsor
University of Minnesota
NCT number
NCT04387422

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 12 Aug 2020 to the primary completion date, Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Uncontrolled hypertension (blood pressure \> 145/95 mmHg at screening)
  • Evidence of autonomic neuropathy (presence of orthostatic hypotension or history of gastroparesis)
  • History of myocardial infarction, stroke, seizures, neurosurgical procedures, major depression requiring hospitalization within the last 5 years, arrhythmias

Lab values

  • Impaired kidney function (GFR \< 45)
  • Use of drugs that can alter glucose metabolism including but not limited to glucocorticoids and niacin, and excluding insulin and glucose lowering drugs used to treat diabetes, as determined by a clinician

Other

  • Impaired awareness of hypoglycemia as determined by the Cox and Gold questionnaires
  • Pregnant or plan to become pregnant during the study period
  • Proliferative retinopathy
  • Current substance abuse
  • Inability to undergo MRI scanning, including but not limited to unable to remain still in an MRI scanner for more than 30 minutes, claustrophobia, presence of paramagnetic substances or pacemakers in body, weight over 300 lbs
  • Unable to complete all study visits or procedures, as determined by the investigator

Who the study is looking for

  • Type 1 diabetes diagnosed on clinical or laboratory grounds
  • Diabetes duration 2 - 30 years
  • Hemoglobin A1C \<8.5%

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.