Status:

TERMINATED

Glucagon Response to Prandial Insulin Administration in Persons With Type 1 Diabetes

Lead Sponsor:

Washington University School of Medicine

Conditions:

Type 1 Diabetes

Hyperglycemia, Postprandial

Eligibility:

All Genders

18-90 years

Phase:

PHASE1

PHASE2

Brief Summary

Glucagon regulation and response in persons with T1D at the basal state and in response to various stimuli remains unclear. Dr. Philip Cryer has previously reported that, in T1D young adults with a co...

Detailed Description

Glucagon regulation and response in persons with T1D at the basal state and in response to various stimuli remains unclear. Dr. Philip Cryer has previously reported that, in T1D young adults with a co...

Eligibility Criteria

Inclusion

  • 10 persons with T1D for \>5 years age \>18.
  • HbA1c \<9.5%
  • Patients using either MDI or insulin pumps will be included.
  • Patients using CGM will continue the use during the study, however glucoses will be measured by laboratory methods.
  • Persons of all races, ethnicity and genders will be included
  • Participants should have normal hemoglobin, hematocrit and eGFR \>60 ml/min/1.73m2.

Exclusion

  • Persons with type 2 diabetes, monogenic diabetes, pancreatic diseases.
  • Pregnancy, prisoners, other vulnerable populations or persons unable to understand the protocol and provide written informed consent.
  • Persons who take daily steroids, any route, for any purpose

Key Trial Info

Start Date :

February 13 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2020

Estimated Enrollment :

1 Patients enrolled

Trial Details

Trial ID

NCT04079881

Start Date

February 13 2020

End Date

July 1 2020

Last Update

October 7 2022

Active Locations (1)

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1

Washington University in St Louis

St Louis, Missouri, United States, 63110