Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00541515
Other study ID # rmc004706ctil
Secondary ID
Status Completed
Phase N/A
First received October 8, 2007
Last updated April 7, 2016
Start date October 2007
Est. completion date September 2015

Study information

Verified date April 2016
Source Rabin Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

An open interventional data collection study in order to build a database to close the loop between glucose sensor and insulin pump.

background: The ultimate goal in diabetes treatment is to develop an autonomous insulin delivery system (artificial pancreas) capable of continuous glucose sensing, thereby mimicking the physiologic function of the islet beta cells and freeing the patient from the need for constant calculations of daily insulin and carbohydrates. Several prototypes of closed-loop system have been developed in recent years, based on different types of control algorithms, to establish the connection between the sensor and the insulin pump. Current research in the formulation of this type of subcutaneous closed-loop system still faces major challenges, therefore, there is a need for further study and evaluation.

Objectives:

1. To evaluate the lag time of the effect of subcutaneous insulin infusion on blood glucose levels by using continuous glucose sensor

2. To measure the insulin sensitivity as expressed by changes in blood glucose levels after s.c insulin infusion .

3. To evaluate real time sensor calibration algorithms based on the measured lag times

4. Collecting clinical data in order to develop and evaluate mathematical models which will serve a base to simulators.

5. Developing and accessing advanced learning and control algorithms as a step towards developing an artificial pancreas


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date September 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Both
Age group 10 Years to 65 Years
Eligibility Inclusion Criteria:

1. Diabetes type 1 for at least one year.

2. ages >10 years.

3. signed informed consent form.

4. willing to cooperate with all study requirements.

Exclusion Criteria:

1. Sensor allergy.

2. Psychiatrist diseases.

3. other chronic diseases.

4. Participation in another study that involves a medicine or a medical device.Subjects have to finish participating in other studies at least 30 days before joining this study. Each subject can participate in this study only once.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
continuous glucose sensors and insulin pump
continuous glucose sensors and insulin pump

Locations

Country Name City State
Israel schneider children medical center of Israel Petach-Tikva

Sponsors (1)

Lead Sponsor Collaborator
Rabin Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood glucose levels countinuasly Yes
See also
  Status Clinical Trial Phase
Active, not recruiting NCT00328302 - Diabetes Type 1, Treatment Study Atacand/Placebo After Kidney Biopsy Phase 4
Completed NCT00810589 - A Randomised, Single Centre, Double-Blind, Two-Period Crossover, Glucose Clamp Trial Phase 1
Completed NCT00046150 - 12 Week,Comparing Safety of HMR1964 & Insulin Aspart Used in Continuous Subcutaneous Infusion in Type 1 Diabetes. Phase 3
Terminated NCT01129232 - Diabetes Virus Detection Project, Intervention With GAD-alum Phase 2
Recruiting NCT00804232 - Childhood Diabetes N/A
Completed NCT00308308 - Efficacy & Safety of Inhaled Insulin in Type 1 Diabetes Phase 3
Completed NCT00654121 - Prevention of Clinical Onset of Type 1 Diabetes in High Risk First Degree Relatives Phase 2
Completed NCT01754259 - Effects of Ranolazine on Coronary Flow Reserve in Symptomatic Diabetic Patients and CAD Phase 3