Amitriptyline in Treating Hypoglycemia

Stopped early · Phase 2 · Has a placebo group

Conditions studied: Type1 Diabetes Mellitus, Hypoglycemia Unawareness

In brief

Patients with type 1 diabetes mellitus (T1DM) commonly experience hypoglycemia and develop impaired awareness of hypoglycemia. Many patients using continuous glucose monitoring (CGM) system to mitigate these complications, but continue to spend a significant amount of time in hypoglycemia. The long-term goal is to develop novel and readily available therapeutic approaches to improve hypoglycemia course and awareness in T1DM patients. The objective of this study is to determine whether amitriptyline will improve hypoglycemia course and the ability to recognize hypoglycemic events in T1DM patients who are using CGM.

Key facts

Study ID

NCT03591458

Run by

University of Utah

People needed

2

Starts

2018-08-01

Expected to finish

2019-06-03

Last updated by the study team

2019-07-22

Who can join

Age: 21 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects with Type 1 Diabetes Mellitus for at least 5 years or more
• Age between 21 to 60 years old
• HbA1c less or equal to 9% with the latest measurement within the last 3 months
• Use of real time Continuous Glucose Monitoring (rtCGM) providing continuous glucose data points for at least 3 months, and at least 80% of CGM readings available over the last 2-week period
• Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines

You may not qualify if…

• Ongoing or recent history of major depressive disorder, or other ongoing major psychiatric disorders
• History of anti-depressant use within the last three months
• Insulin pump linked to a CGM with programmed automatic insulin adjustment or suspension
• History of advanced cardiac, liver, kidney or neurological disease
• Active malignancy
• Uncontrolled Human Immunodeficiency Virus diseases
• Advanced diabetic retinopathy, neuropathy, or nephropathy
• Frequent acetaminophen use which can disrupt CGM accuracy
• Pregnancy or female of child-bearing potential unable to practice effective contraception during the study period
• Breastfeeding female, or female with prospective plan to initiate breastfeeding
• Ongoing history of alcohol abuse
• Contraindication to amitriptyline use, including hypersensitivity to amitriptyline or any component of the formulation, co-administration with or within 14 days of Monoamine Oxidase Inhibitors and co-administration with cisapride
• Inability to understand or cooperate with study procedures, including taking study drugs and recording hypoglycemic symptoms.
• The participants meeting the above criteria will enter "Run-in Period". At the Visit 2, the following additional exclusion criteria will be applied before study drug randomization:
• < 80% of CGM readings available over the last 2-week period
• Time spent in hypoglycemia (i.e., < 70 mg/dL) for < 5% over a 2-week period on based on CGM reading.

Where it is running

• University of Utah — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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