Insulin Lispro 6 Days Versus Insulin Aspart 6 Days in Pump Use
Status: | Completed |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 13 - Any |
Updated: | 3/29/2019 |
Start Date: | April 2010 |
End Date: | August 2011 |
An Open-Label, Randomized, Crossover Trial of CSII Reservoir In-use Comparing Insulin Lispro Formulation to Insulin Aspart in Patients With Type 1 Diabetes Mellitus
This is a 6-sequence, 3-period (8 weeks each), 3-arm, 24-week crossover study. The purpose of
this study is to provide information on the use of insulin lispro in insulin pumps
(Continuous Subcutaneous Insulin Infusion [CSII]) compared to insulin aspart over 6 days of
pump reservoir in-use. The study will also compare the in-use characteristics of insulin
lispro infused at 6 days with insulin lispro infused at 2 days.
this study is to provide information on the use of insulin lispro in insulin pumps
(Continuous Subcutaneous Insulin Infusion [CSII]) compared to insulin aspart over 6 days of
pump reservoir in-use. The study will also compare the in-use characteristics of insulin
lispro infused at 6 days with insulin lispro infused at 2 days.
Inclusion Criteria:
- Diagnosed with type 1 diabetes (World Health Organization criteria) for at least 24
months.
- Treated with continuous subcutaneous insulin infusion therapy for the previous 6
months.
- Mean total daily insulin dose for 3 days prior to screening equal to or less than 46
units/day using a 300-unit reservoir or less than or equal to 26 units/day using a 180
unit reservoir.
- Baseline body mass index (BMI) less than or equal to 35.0 kg/m^2.
- Baseline glycosylated hemoglobin (HbA1c) 5% to 9%.
Exclusion Criteria:
- Impaired renal function (serum creatinine greater than or equal to 2.0 milligrams per
deciliter [mg/dL]).
- Legal blindness.
- Have had any episode of hypoglycemic coma, seizures, or disorientation in the 12
months prior to screening.
- Have had hypoglycemia unawareness (routinely asymptomatic at blood glucose (BG) less
than 45 mg/dL) in the 12 months prior to screening.
- Have had any emergency room visits or hospitalizations due to poor glucose control in
the 12 months prior to screening.
- Have had a pump-related infusion site abscess in the 12 months prior to screening.
- Have had multiple, clinically significant occlusions as judged by the investigator.
- Have had any infection with staphylococcus aureus in the past 5 years.
- Have one of the following concomitant diseases: presence of clinically significant
hematologic, oncologic, renal, cardiac, hepatic, or gastrointestinal disease, or any
other serious disease considered by the investigator to be exclusionary.
- Patients with malignancy other than basal cell or squamous cell skin cancer who have
not yet been treated, are currently being treated, or who were diagnosed less than 5
years ago.
- Have had a blood transfusion or severe blood loss within 3 months prior to screening,
or have known hemoglobinopathy, hemolytic anemia or sickle cell anemia, or any other
traits of hemoglobin abnormalities known to interfere with HbA1c methodology.
- Are receiving chronic (lasting longer than 14 consecutive days) systemic
glucocorticoid therapy (excluding topical, intra-articular, intraocular and inhaled
prescriptions), or have received such therapy within the 4 weeks immediately preceding
screening.
- Have an irregular sleep/wake cycle (for example, patients who sleep during the day and
work during the night), in the investigator's opinion.
- Have known hypersensitivity or allergy to any of the study insulins or their
excipients.
- Are breastfeeding or pregnant, or intend to become pregnant during the course of the
study, or are sexually active women of childbearing potential not actively practicing
birth control by a method determined by the investigator to be medically acceptable.
- Are currently enrolled in, or discontinued within the last 30 days from, a clinical
trial involving an off-label use of an investigational drug or device (other than the
study drug/device used in this study), or concurrently enrolled in any other type of
medical research judged not to be scientifically or medically compatible with this
study.
- Have previously completed or withdrawn from this study after having signed the
informed consent document (ICD).
- Are unwilling or unable to comply with the use of a data collection device to directly
record data from the patient.
We found this trial at
11
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials