Trial Search Results

Hyaluronidase Effect on Infusion Set Life

This research study examines the effect of hyaluronidase on the length of time of insulin infusion set wear. The aim of the study is to improve the length of time that an infusion set can be worn by infusing hyaluronidase directly into the insulin infusion site. The investigators will also assess the accuracy of the Dexcom G4 Platinum (G4P) sensors with extended sensor wear beyond the 7 day FDA approved time frame.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Stanford University

Collaborator: University of Colorado Denver School of Medicine Barbara Davis Center

Stanford Investigator(s):

Intervention(s):

  • Drug: Hyaluronidase

Phase:

Phase 2/Phase 3

Eligibility


Inclusion Criteria:

   1. Clinical diagnosis of type 1 diabetes for at least one year and using an insulin pump
   for at least 3 months

   2. Total daily insulin dose of at least 0.4 units/kg/day

   3. The diagnosis of type 1 diabetes is based on the investigator's judgment; C peptide
   level and antibody determinations are not needed.

   4. Age 12 to 45 years

   5. Hemoglobin A1c level less than or equal to 10%

   6. Willingness to infuse 1 ml of hyaluronidase (Hylenex) into the insulin infusion set
   after insertion on day 1 and day 3 of the week they are assigned to use hyaluronidase

   7. Willingness to use a Silhouette or Comfort insulin infusion set throughout the study.
   The set includes the Duo Infusion Tubing for infusion of hyaluronidase (Hylenex).

   8. Willingness to eat the same breakfast each morning for the first two weeks of the
   study

   9. Willing to take two 500mg tablets of Tylenol Regular Strength and monitor glucose
   levels at ½, 1, 2, 4, 6, and 8 hours later.

10. For females, not currently known to be pregnant

11. An understanding of and willingness to follow the protocol and sign the informed
   consent

12. Must be able to understand spoken or written English

Exclusion Criteria:

   1. Diabetic ketoacidosis in the past 6 months

   2. Severe hypoglycemia resulting in seizure or loss of consciousness in the 6 months
   prior to enrollment

   3. Known tape allergies

   4. Current treatment for a seizure disorder

   5. Cystic fibrosis

   6. Active infection

   7. A known medical condition that in the judgment of the investigator might interfere
   with the completion of the protocol such as the following examples:

   8. Inpatient psychiatric treatment in the past 6 months for either the subject or the
   subject's primary care giver (i.e., parent or guardian)

   9. Presence of a known adrenal disorder

10. If on antihypertensive, thyroid, anti-depressant or lipid lowering medication, lack of
   stability on the medication for the past 2 months prior to enrollment in the study

11. Abuse of alcohol

12. Use of an OmniPod insulin infusion pump

13. Pregnant or lactating females

Ages Eligible for Study

12 Years - 45 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