Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Baltimore, Maryland 21201


Purpose:

This study is aimed at determining if the drug Atomoxetine (Strattera-used to treat Attention Deficit Hyperactivity Disorder(ADHD) has effects on the body's ability to defend itself against low blood sugar.


Study summary:

The purpose of this study is to see if the drug atomoxetine (Strattera) has effects on the body's ability to defend itself against low blood sugar. Normally, when blood sugar levels drop below normal, the body creates a series of responses, which increase the sugar inside the body to bring blood sugar levels back to normal. The hormone epinephrine is a key defense against low blood sugar in people with diabetes. Atomoxetine has been shown to increase this hormone level. Thus, any approaches to increase levels of this key defense during low blood sugar may have great value.


Criteria:

Inclusion Criteria: - Healthy individuals aged 18-50 years - Type 1 Diabetes individuals aged 18-50 years - BMI <40 kg/m2 - Females of childbearing potential with negative urine pregnancy test - Volunteers over 40 years of age, a cardiac stress test with no clinically significant conduction or ischemic changes Exclusion Criteria: The following groups of subjects will be excluded from the study: - Pregnant women - Subjects unable to give voluntary informed consent - Subjects on anticoagulant drugs or with known bleeding diatheses - Subjects with uncontrolled hypertension, heart disease, cerebrovascular incidents - Subjects taking MAOIs - Subjects with narrow angle glaucoma - Subjects with diagnosed psychiatric disorders - Subjects with allergy to atomoxetine, heparin, or lidocaine Physical Exam Exclusion Criteria: - Uncontrolled severe hypertension (i.e., blood pressure greater than 150/95) - 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 - Renal Failure - Acute Cerebrovascular/ Neurological deficit - Fever greater than 38.0 C Screening Laboratory Tests Exclusion Criteria Blood values as defined in protocol


NCT ID:

NCT00780650


Primary Contact:

Principal Investigator
Stephen N. Davis, MD
University of Maryland, Baltimore


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21201
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.