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Clinical Trials/NCT01672255
NCT01672255
Completed
Early Phase 1

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

University of Maryland, Baltimore1 site in 1 country64 target enrollmentOctober 1, 2012

Overview

Phase
Early Phase 1
Intervention
Fluoxetine
Conditions
Type 1 Diabetes
Sponsor
University of Maryland, Baltimore
Enrollment
64
Locations
1
Primary Endpoint
Change in Catecholamines
Status
Completed
Last Updated
6 months ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
October 1, 2012
End Date
May 1, 2025
Last Updated
6 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stephen N. Davis, MBBS

Principal Investigator

University of Maryland, Baltimore

Eligibility Criteria

Inclusion Criteria

  • 32 (16 males, 16 females) Healthy controls aged 18-45 yr.
  • 32 (16 males, 16 females) Type 1 diabetic patients aged 18-45 yr.
  • HbA1c 6-10.0%
  • Has been diagnosed Type 1 DM
  • No clinically diagnosed diabetic tissue complications (i.e. history of retinopathy, neuropathy, stasis ulcers, etc)
  • Body mass index \< 40kg • m-2

Exclusion Criteria

  • Pregnant women
  • 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
  • Subjects with a history of hypertension, heart disease, cerebrovascular incidents
  • Current tobacco use

Arms & Interventions

Trial 1-SSRI

90 minute exercise baseline with 6 weeks treatment with SSRI (Prozac). Repeat 90 minute exercise after 6 week treatment.

Intervention: Fluoxetine

Trial 2-Placebo

90 minute exercise at baseline with 6 weeks treatment with placebo. Repeat 90 minute exercise after 6 weeks treatment of placebo.

Intervention: Placebo control

Outcomes

Primary Outcomes

Change in Catecholamines

Time Frame: During 90 minute experimental period

This change in catecholamines will be compared to another 90 minute experimental period after 8 weeks administration of SSRI or placebo.

Study Sites (1)

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