Trial Search Results

Testing State of the Art Remote Glucose Monitoring at Diabetes Camp

The incidence of low blood sugar and hypoglycemic seizures at diabetes camp has been reduced thanks to overnight blood glucose level testing. The timing of the overnight blood test is often arbitrary and it is unclear when the highest frequency of nocturnal hypoglycemic events at camp are occurring. It is also unclear what the most appropriate treatment for nocturnal hypoglycemia is: simple carbohydrates, or mini-glucagon.

In this study, we will use Continuous Glucose Monitors (CGMs) that will send subject data securely to a remote computer located in the medical cottage at camp throughout the night. Study staff will monitor the computer and will intervene on low blood sugar as it occurs in real time. On half of the nights, campers will receive mini-glucagon for low blood sugar, and on the rest, they will receive standard carbohydrate treatment.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Stanford University

Collaborator: The Leona M. and Harry B. Helmsley Charitable Trust

Stanford Investigator(s):

Intervention(s):

  • Drug: Mini-glucagon
  • Device: Remote monitoring
  • Dietary Supplement: Carbohydrates

Phase:

N/A

Eligibility


Inclusion Criteria:

   - Clinical diagnosis of type 1 diabetes and using daily insulin therapy for at least one
   year

   - Age 7-21 years

   - Attendee of Camp De Los Ninos or Conrad Chinnock

   - Come to camp with a consent already signed after having talked to study staff about
   the study, or at the onset of the camp meet with study staff and sign the consent
   before the first night at camp.

   - Using multiple daily insulin injections (Lantus) or on an insulin pump (any brand)

Exclusion Criteria:

   - Cystic fibrosis

   - Medications such as current use of oral steroids or other medications, which in the
   judgment of the investigator would be a contraindication to participation in the
   study.

   - History of adhesive allergies which would interfere with sensor wear.

Ages Eligible for Study

7 Years - 21 Years

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Not Recruiting