The Effect of Bolus Speed of Rapid-Acting Insulin Analog Absorption and Action in Individuals With Type 1 Diabetes
Status: | Recruiting |
---|---|
Conditions: | Diabetes, Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 30 |
Updated: | 6/20/2018 |
Start Date: | May 30, 2018 |
End Date: | December 31, 2019 |
Contact: | Lori Carria |
Email: | lori.carria@yale.edu |
Phone: | 203-737-3595 |
The Effect of Insulin Bolus Speed of Rapid-Acting Insulin Analog Absorption and Action in Individuals With Type 1 Diabetes
Rapid Action Insulin (RAI) absorption and action measured by time to reach maximum insulin
concentration and glucose infusion rate.
concentration and glucose infusion rate.
The investigators hypothesize that RAI absorption and action measured by time to reach
maximum insulin concentration and glucose infusion rate during the clamp study will be
significantly faster when insulin bolus is delivered using the "Quick Bolus" feature as
compared to the "Standard Bolus".
maximum insulin concentration and glucose infusion rate during the clamp study will be
significantly faster when insulin bolus is delivered using the "Quick Bolus" feature as
compared to the "Standard Bolus".
Inclusion Criteria:
1. Age 18 - 30 (inclusive)
2. Clinical diagnosis of T1D of at least one year's duration
3. On Continuous Subcutaneous Insulin Infusion (CSII) therapy for at least three months
4. HbA1c <10%
5. Minimum weight requirement of at least 37.9 kg
6. Ability to comprehend written and spoken English
7. Total daily requirement of insulin between 0.6 and1.2 U/kg/day
8. Not have any other medical condition or disease known to affect insulin action and
glucose control aside from T1D or treated hypothyroidism
Exclusion Criteria:
1. Medication besides insulin known to alter blood glucose or insulin action
2. Female subjects of reproductive potential that are pregnant or breast feeding, or not
consistently using a barrier method or abstinence as contraception.
3. Inability to comprehend written and spoken English
4. Any other condition, which in the judgment of the investigators, would interfere with
the subject's ability to provide informed consent or the investigator's ability to
perform the study
5. Hematocrit less than 35% or a serum potassium less than 3.4 mmol/L
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