MedPath

AchE Inhibitor and Insulin

Phase 1
Completed
Conditions
Diabetes Mellitus
Interventions
Registration Number
NCT03063515
Lead Sponsor
University of Miami
Brief Summary

The investigator will examine the effect of a single dose of pyridostigmine, AchE inhibitor on insulin secretion in healthy subjects. Each subject will undergo an intravenous glucose tolerance test (IVGTT) where IV glucose will be administered and the glucose excursion and insulin secretion response will be evaluated by measuring insulin and glucose at different time points. The test will be carried out twice, once without and once with the administration of a single dose of Pyridostigmine on two separate days. The investigator hypothesizes that inhibiting AChE will potentiate insulin secretion.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria
  • 18 years and older
Exclusion Criteria
  • BMI >30 Kg/m2
  • fasting glucose >100
  • Glycohemoglobin (Hemoglobin A1C) 5.7% or more
  • History of asthma
  • Use of medications that may interfere with glucose metabolism

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
IVGTT with pyridostigminePyridostigmineAn IVGTT will be performed 2 hours after taking one single dose of pyridostigmine 60 mg
Primary Outcome Measures
NameTimeMethod
First phase insulin response to IV glucose infusion-10, -4, 1, 2, 3, 4, 5, 6, 8, and 10 minutes

Insulin positive incremental area under the curve and the sum of plasma insulin values at 1 minute and 3 minutes after IV glucose infusion

Secondary Outcome Measures
NameTimeMethod
Glucose excursion after IV glucose infusion-10, -4, 1, 2, 3, 4, 5, 6, 8, and 10 minutes

Glucose positive incremental area under the curve

Trial Locations

Locations (1)

Diabetes Research Institute

🇺🇸

Miami, Florida, United States

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