The Effects of Fluoxetine and/or DHEA



Status:Recruiting
Conditions:Diabetes, Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 50
Updated:2/2/2019
Start Date:December 19, 2017
End Date:December 10, 2020
Contact:Maka S Hedrington, MD
Email:mhedrington@som.umaryland.edu
Phone:410-706-5623

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The Effects of the Selective Serotonin Reuptake Inhibitor, Fluoxetine and/or DHEA, on Neuroendocrine, Autonomic Nervous System and Metabolic Counterregulatory Responses During Repeated Hypoglycemia in T1DM Individuals

(1) To determine how the Selective Serotonin Reuptake Inhibitor (SSRI), fluoxetine (Prozac),
an antidepressant often used to treat depression, stimulates the participant's body's ability
to defend against low blood sugar (hypoglycemia). (2) To learn how a hormone,
dehydroepiandrosterone (DHEA), stimulates the participant's body's ability to defend itself
from low blood sugar (hypoglycemia). DHEA is a hormone produced naturally in the human body.
However, it can be manufactured and is sold as an over-the-counter dietary supplement. The
dose the investigators are giving in this study is higher than the usual recommended dosage
taken as a supplement for certain medical conditions. (3) To study combined effects of
fluoxetine and DHEA during low blood glucose. In the present study, the investigators will
measure the participant's body's responses to hypoglycemia when given fluoxetine or DHEA or
fluoxetine and DHEA or a placebo (a pill with no fluoxetine or DHEA). Approximately 64
individuals with type 1 diabetes will take part in this study.


Inclusion Criteria:

- 64 (32 males, 32 females) T1DM patients aged 18-50 yr.

- HbA1c < 11.0%

- No clinically diagnosed diabetic tissue complications (i.e. history of retinopathy,
neuropathy, stasis ulcers, etc)

- Body mass index < 40kg · m-2

Exclusion Criteria:

- Pregnancy

- Subjects unable to give voluntary informed consent

- Subjects on anticoagulant drugs, anemic or with known bleeding diatheses

- Subjects taking any of the following medications will be excluded: Non-selective Beta
Blockers, Sedative-Hypnotics, Anticonvulsants, Antiparkinsonian drugs, Antipsychotics,
Antidepressants, Mood stabilizers, CNS Stimulants, Opioids, Hallucinogens

- Subjects with a recent medical illness or past history of severe depression, mania or
psychotic disease

- Subjects that score greater than 50 on the depression scale

- Subjects unwillingness or inability to comply with approved contraception measures

- Abnormal results following screening tests and physical examination that are
clinically significant

- Subjects with a history of severe uncontrolled hypertension (i.e., blood pressure
greater than 160/100), heart disease, cerebrovascular incidents

- Clinically significant cardiac abnormalities (e.g. heart failure, arrhythmias,
ischemic tachycardia, S-T segment deviations, etc.) from history or from cardiac
stress testing in subjects ≥ 40 years old.

- Pneumonia

- Hepatic Failure/Jaundice

- Creatinine greater than 1.6 mg/dl

- Acute Cerebrovascular/ Neurological deficit

- Fever greater than 38 °C

Screening Laboratory Tests Exclusion Criteria

- Hematocrit lower than 32

- WBC lower than 3 thou/ul or greater than 14 thou/ul

- Liver Function Tests: SGOT and SGPT greater than twice upper limit of normal range
(i.e. greater than 80 U/L).

- TBil greater than 2 mg/dl

- Alkaline Phosphatase greater than 150U/L

- Positive HIV, Hep B, Hep C

- Hepatic transaminase > 2x normal
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Phone: 410-706-5623
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