Closed-Loop With Faster Aspart in Young Adults With Type 1 Diabetes

NCT ID: NCT03212950

Last Updated: 2017-11-06

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

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-07-10

Study Completion Date

2017-11-01

Brief Summary

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A randomized, double-blinded (for insulin type), single centre, crossover design young adult study, on 20 subjects with type 1 diabetes (T1D), aged 18 to 25 (inclusive) years, measuring time in glucose values within 3.9 - 10 mmol/l (70-180 mg/dl) under supervision of DreaMed Glucositter using either faster-acting insulin Aspart (Fiasp®, European Medicines Agency number EMEA/H/C/004046) or normal acting insulin Aspart.

Study duration will be about 3 weeks per subject, 5 month overall.

The objectives of this clinical investigation is:

1\. to evaluate the safety and efficacy of blood glucose control using the DreaMed Glucositter with Fiasp® in young adults with T1D during and after unannounced afternoon physical activity and unannounced meals, in a controlled in-hospital environment.

Primary endpoint is significant between-group difference (intervention Fast-CL versus control Regular-CL) in time within range of glucose values within 3.9 - 10 mmol/l (70-180 mg/dl) during the unannounced afternoon exercise and unannounced standardized meals from 15:00 till 18:00 next day based on sensor glucose readings.

Detailed Description

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Conditions

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Type 1 Diabetes Mellitus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Fast-CL

Glucose control using DreaMed Glucositter and Fiasp® (Fast-CL)

Group Type EXPERIMENTAL

Fast-CL

Intervention Type DRUG

After the admission we will insert new insulin (blinded) into the insulin pump. At 13:00 they will have lunch (with manual bolus). At 15:00 we will start CL control, participants/investigators will not be allowed to deliver manual bolus till the end of the study period. All meals and afternoon exercise (in the time between 16:30 and 19:30) will be unannounced and managed with CL.

Regular-CL

Glucose control using DreaMed Glucositter and regular insulin Aspart

Group Type ACTIVE_COMPARATOR

Regular-CL

Intervention Type DRUG

After the admission we will insert new insulin (blinded) into the insulin pump. At 13:00 they will have lunch (with manual bolus). At 15:00 we will start CL control, participants/investigators will not be allowed to deliver manual bolus till the end of the study period. All meals and afternoon exercise (in the time between 16:30 and 19:30) will be unannounced and managed with CL.

Interventions

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Fast-CL

After the admission we will insert new insulin (blinded) into the insulin pump. At 13:00 they will have lunch (with manual bolus). At 15:00 we will start CL control, participants/investigators will not be allowed to deliver manual bolus till the end of the study period. All meals and afternoon exercise (in the time between 16:30 and 19:30) will be unannounced and managed with CL.

Intervention Type DRUG

Regular-CL

After the admission we will insert new insulin (blinded) into the insulin pump. At 13:00 they will have lunch (with manual bolus). At 15:00 we will start CL control, participants/investigators will not be allowed to deliver manual bolus till the end of the study period. All meals and afternoon exercise (in the time between 16:30 and 19:30) will be unannounced and managed with CL.

Intervention Type DRUG

Other Intervention Names

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Faster Acting Insulin Aspart and DreaMed Glucositter Insulin Aspart and DreaMed Glucositer

Eligibility Criteria

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Inclusion Criteria

1. The subject has documented T1D, as defined by the American Diabetes Association and World Health Organization (ADA/WHO) for at least 1 year prior to study enrolment
2. Documented evidence should exist within the patient history of T1D
3. The subject is between 18 and 25 years of age (inclusive) at the time of enrolment
4. The subject has been treated with an insulin pump for at least 3 months
5. The subject has an A1C value ≤ 9% based on analysis from the local laboratory at the time of enrolment

● A1C testing must follow National Glycohemoglobin Standardization Program (NGSP) standards.
6. The subject is willing to follow all study instructions
7. Subject is available for the entire study duration and follow-up visits
8. Subject is willing to perform daily self-monitoring of blood glucose (SMBG) and required sensor calibrations
9. If subject has celiac/Hashimoto disease, the disease has to be adequately treated as determined by the investigator
10. Subject has a BMI above 5th centile and below 95th centile for age, respectively.

Exclusion Criteria

1. Concomitant diseases that influence metabolic control (e.g. anemia, significantly impaired hepatic function, renal failure, history of adrenal insufficiency) or other medical conditions, which in the investigator's opinion, may compromise patient safety; Note: Adequately treated thyroid disease and celiac disease do not exclude subjects from enrollment.
2. Significant co-morbidity that, in the opinion of the investigators would preclude participation in the study (e.g. current treatment for cancer, mental disorder)
3. Subject is taking or has taken oral or parenteral glucocorticoids within 1 month prior to screening, or plans to take oral or parenteral glucocorticoids during the study. Exceptions: Short term oral glucocorticoids up to 7 days, inhaled steroids.
4. Subject is taking antidiabetic agents or other medications, which could be a contraindication to participation in the study by the judgment of the investigator.
5. Subject is participating in another study of a medical device or drug that could affect glucose measurements or glucose management or Receipt of any investigational medical product within 1 month prior to screening (Visit 1).
6. Female subject of child-bearing potential who is pregnant, breast-feeding, or planning to become pregnant during the study.
7. Subject has a history of one or more episodes of Diabetic Ketoacidosis (DKA) requiring hospitalization within a month prior to the screening.
8. Subject has current or recent history of alcohol or drug abuse.
9. Subject has visual impairment or hearing loss, which in the investigator's opinion, may compromise patient ability to perform study procedures safely (child and parent should be evaluated as a unit).

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Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Ljubljana, Faculty of Medicine

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tadej Battelino, Prof, MD

Role: PRINCIPAL_INVESTIGATOR

University of Ljubljana, Faculty of Medicine

Locations

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UMC-University Children's Hospital

Ljubljana, , Slovenia

Site Status

Countries

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Slovenia

References

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Other Identifiers

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PD-FAST-01

Identifier Type: -

Identifier Source: org_study_id