CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 30 enrolled
Drug / intervention
Naloxone then placebo +1 moredrug
Likely dose
Naloxone then placebo 4mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03149770
NCT03149770Phase 2Completed

Hypoglycemia After Exercise in Type 1 Diabetes: Intranasal Naloxone as a Novel Therapy to Preserve Hypoglycemia Counterregulation

University of Minnesota·interventional·Posted May 11, 2017·Updated Apr 16, 2024

In Brief

A Phase 2 clinical trial evaluating Naloxone then placebo and Placebo then Naloxone for Diabetes Mellitus, Type 1. Completed, enrolled 30 participants across 1 site.

Detailed Summary

The overall objective of this project is to determine if the intranasal administration of naloxone during exercise will be a novel approach to preserve the counterregulatory response to hypoglycemia experienced the next day in patients with type 1 diabetes. Exercise induced autonomic failure contributes to the development of impaired awareness of hypoglycemia. Treatments that blunt the consequences of exercise induced autonomic failure, such as preserving the post-exercise counterregulatory response to hypoglycemia, may improve awareness of hypoglycemia. Naloxone, an opioid antagonist, is an extremely promising agent. In healthy volunteers, intravenous administration of naloxone during exercise preserved the counterregulatory response to hypoglycemia the following day (1). In this study, investigators will extend the clinical applicability by administering intranasal naloxone to individuals with type 1 diabetes. Specifically, the investigators will use a randomized, placebo controlled, crossover design to administer drug or placebo to patients with type 1 diabetes during acute exercise and assess the counterregulatory response to hypoglycemia the following day. The use of intranasal naloxone is a highly innovative aspect of this proposal. Intranasal naloxone translates readily to clinical use and, as demonstrated by the investigators preliminary data, achieves similar plasma drug concentrations as after IV administration.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedMay 11, 2017
Enrollment StartSep 18, 2017
Primary CompletionMay 1, 2022
Study CompletionApr 1, 2023
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 9.1 years ago

Interventions

Naloxone then placebodrug

naloxone intranasal 4mg, then placebo

Placebo then Naloxonedrug

placebo then naloxone intranasal 4mg