Closed Loop Insulin Therapy in Type 1 Diabetics Based on Blood Microdialysis, Online Sensors and an eMPC Algorithm

NCT ID: NCT00535483

Last Updated: 2014-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

4 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-08-31

Study Completion Date

2007-09-30

Brief Summary

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The EU funded project CLINICIP (Closed Loop Insulin Infusion for Critically Ill Patients) aims to develop a low-risk monitoring and control device which allows maintaining metabolic control in intensive care units. A system will be developed comprising three subsystems: a body interface for the delivery of biofluids, biosensors for the determination of glucose concentration in these biofluids and an adaptive control algorithm that generates advice and thus represents a decision support system with respect to insulin infusion rate to establish glycaemic control in critically ill patients. Within a closed loop system, intensified insulin treatment will make use of the calculations leading to external regulation of glucose.

It is the aim of this study to evaluate the feasibility to establish glycaemic control in type 1 diabetic subjects over a period of 30 hours by manually combining these three - previously tested - subsystems (ABS System, extracorporeal online glucose sensor and a laptop-based computer algorithm).

Detailed Description

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Conditions

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Type 1 Diabetes

Study Design

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Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Signed informed consent obtained before any trial-related activities
* Age of analysable subjects in the range from 18 to 65 years
* Type 1 diabetes (Treatment with multiple daily injection for more than 12 months)

Exclusion Criteria

* Severe acute and/or chronic diseases
* Mental incapacity, unwillingness or language barriers precluding adequate understanding or co-operation
* Taking of any vasoactive substances or anticoagulation medication.
* Diseases of the skin which could interfere with application of the catheters.
* Pregnancy or breastfeeding
* Bleeding disorder
* Known heparin allergy or heparin intolerance
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medical University of Graz

OTHER

Sponsor Role lead

Principal Investigators

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Thomas R Pieber, MD

Role: PRINCIPAL_INVESTIGATOR

Medical University Graz, Graz, Austria

Locations

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Medical University Graz - Clinical Research Center

Graz, Styria, Austria

Site Status

Countries

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Austria

Related Links

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http://www.joanneum.at/health

http://www.joanneum.at/health

Other Identifiers

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ABS3

Identifier Type: -

Identifier Source: org_study_id

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