Clinical Trials Directory

Trials / Completed

CompletedNCT01672255

Hypoglycemia Associated Autonomic Failure in Type 1 Diabetes Mellitus (DM)

Hypoglycemia Associated Autonomic Failure in Type 1 DM, SSRI and Exercise

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
64 (estimated)
Sponsor
University of Maryland, Baltimore · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Exercise is a cornerstone of diabetes management. It helps reduce blood pressure, promote weight loss, lower insulin resistance and improve glucose and lipid (triglyceride and HDL-cholesterol) profiles. Unfortunately, the benefits of exercise are often not embraced by diabetic individuals because of the fear of low blood sugar (hypoglycemia). My laboratory has demonstrated that Autonomic nervous system (ANS) counterregulatory failure plays an important role in exercise associated hypoglycemia in Type 1 DM. ANS responses are significantly reduced in Type 1 DM and are further blunted by antecedent episodes of hypoglycemia. Furthermore, there is a large sexual dimorphism of reduced ANS responses during submaximal exercise in both Type 1 DM and healthy individuals that is unexplained. Accumulating data are demonstrating that serotonergic pathways can regulate ANS discharge. Generally, serotonergic pathways are inhibitory but both single and longer term administration of selective serotonin reuptake inhibitors (SSRI's) such as Prozac has been demonstrated to increase basal epinephrine levels and enhance baroreflex control of Sympathetic nervous system (SNS) activity. What is unknown is whether fluoxetine can also enhance SNS responses and also override the large ANS sexual dimorphism present during sub maximal exercise. Therefore, the purpose of this study is to determine if the SSRI fluoxetine (Prozac) can improve SNS responses during exercise.

Conditions

Interventions

TypeNameDescription
DRUGFluoxetine20 mg week 1, 40 mg week 2, 60 mg week 3, 80 mg week 4-6
DRUGPlacebo control20 mg Week 1, 40 mg Week 2, 60 mg Week 3, 80 mg Week 4-6

Timeline

Start date
2012-10-01
Primary completion
2025-05-01
Completion
2025-05-01
First posted
2012-08-24
Last updated
2025-10-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01672255. Inclusion in this directory is not an endorsement.