Investigation of the Impact of Different Application Volumes of Insulin Aspart in Subjects With Type 1 Diabetes
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|ClinicalTrials.gov Identifier: NCT01399346|
Recruitment Status : Completed
First Posted : July 21, 2011
Last Update Posted : April 20, 2012
Rationale: For the development of a closed loop system, faster insulin absorption after bolus administration could help to reduce the system's delay and thus increase patient safety. It has been shown that regular insulin absorption is faster when injecting insulin with a sprinkler needle (containing holes in the walls and being sealed at the tip). The current study will evaluate the impact of different application volumes on pharmacokinetic and pharmacodynamic properties of rapid acting insulin analogue (insulin aspart).
Objective: To compare the pharmacokinetic response (based on the time to maximum observed serum insulin concentration) and pharmacodynamic properties of rapid acting insulin aspart after subcutaneous injection of a defined dose (volume) at 1 versus 9 injection sites in patients with type 1 diabetes.
Study design: Monocentric, randomised, controlled, two-arm cross-over intervention study.
Population: Twelve type 1 diabetic subjects
Intervention: The investigational treatment is the subcutaneous administration of insulin aspart either as one bolus of 18 IU at one injection site or as 9 separately and simultaneously applied bolus of 2 IU each at 9 separate injection sites. Serum and plasma samples to assess pharmacodynamic and pharmacokinetic properties will be taken during an 8-hour clamp experiment. Patients will undergo both investigational treatments in a randomized order; between the two clamp visits there will be a wash-out period of 5-21 days.
Main study endpoint: Time to maximum observed serum insulin aspart concentration.
|Condition or disease||Intervention/treatment||Phase|
|Type 1 Diabetes||Drug: Insulin aspart||Phase 1|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||12 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Basic Science|
|Official Title:||A Single-center, Randomized, Controlled, 2-period Cross-over, Open-labelled Trial to Evaluate the Impact of Different Application Volumes on Pharmacokinetic and Pharmacodynamic Properties of Insulin Aspart in Subjects With Type 1 Diabetes|
|Study Start Date :||April 2011|
|Actual Primary Completion Date :||June 2011|
|Actual Study Completion Date :||June 2011|
Experimental: 1 bolus of insulin aspart 18 IU
Subcutaneous administration of insulin aspart as one bolus of 18 IU at one injection site.
Drug: Insulin aspart
Application of 18 IU insulin aspart as one bolus at one injection site
Experimental: 9 bolus of insulin aspart a 2 IU
Subcutaneous administration of insulin aspart as 9 separately and simultaneously applied bolus of 2 IU at 9 separate injection sites
Drug: Insulin aspart
Application of 18 IU insulin aspart as 9 bolus of 2 IU each at nine injection sites
- tmax(ins), time to maximum observed serum insulin aspart concentration [ Time Frame: 8 hours ]
- t10%max(ins), time to reach 10% of maximum observed serum insulin aspart concentration [ Time Frame: 8 hours ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01399346
|Medical University of Graz|
|Graz, Austria, 8036|
|Principal Investigator:||Thomas R Pieber, MD||Medical University of Graz|