Comparison of Insulins Aspart and Lispro in Insulin Pumps
Completed · Phase 4
Conditions studied: Type 1 Diabetes Mellitus
In brief
The purpose of the study is to compare the glycemic control between insulins aspart and lispro 48 to 100 hours after pump infusion line change in subjects with type 1 using diabetes using an insulin pump.
Key facts
- Study ID
- NCT00461331
- Run by
- Tulane University Health Sciences Center
- People needed
- 20
- Starts
- 2004-10-01
- Expected to finish
- 2008-08-01
- Last updated by the study team
- 2021-01-08
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Type 1 Diabetes treated with a pump for at least 3 months
You may not qualify if…
- Pregnancy
- Plasma Creatinine > 1.2 mg/dl
- Inability to give informed consent
- HbA1c > 8%
- Known or suspected hypersensitivity to trial drugs or any of their components
Where it is running
- Clinical Translational Unit - Tulane School of Medicine — New Orleans, Louisiana, United States
Full record on ClinicalTrials.gov
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