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Clinical Trials/NCT03579615
NCT03579615
Completed
Not Applicable

An Open-label, Single-centre, Randomised, Two-period, Cross-over Study to Assess the Efficacy and Safety of Day and Night Automated Closed-loop Glucose Control for 24 Hours in Adults With Type 1 Diabetes Comparing Faster-acting Insulin Aspart With Insulin Aspart

Manchester University NHS Foundation Trust1 site in 1 country18 target enrollmentDecember 23, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 1
Sponsor
Manchester University NHS Foundation Trust
Enrollment
18
Locations
1
Primary Endpoint
Time spent in the target glucose range
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The main objective of the study is to determine whether automated closed-loop using faster-acting insulin aspart will improve glucose control and reduce the burden of hypoglycaemia over a 23-hour period compared to insulin aspart under conditions mimicking under-estimation of meal carbohydrate content or missed meal bolus. Faster-acting insulin aspart (FIASP) is a novel formulation of insulin aspart in which two additional excipients (L-arginine and Niacinamide) have been added, resulting in accelerated initial absorption and more than double the glucose lowering effect in the first 30 minutes after subcutaneous administration using insulin pump. To date, no closed-loop study has been performed to evaluate the benefit of faster-acting aspart over insulin aspart during closed-loop system use.

Detailed Description

This is an open-label, single-centre, two-period, randomised, cross over study. The study involves a screening visit to assess participant eligibility and two 24 hour in-patient stays at the clinical research facility during which day and night glucose levels will be controlled by the closed-loop system with either faster-acting insulin aspart or insulin aspart. Up to 22 adults with type 1 diabetes and treated with continuous subcutaneous insulin infusion will be recruited, aiming for 16 completed participants. Recruitment will take place at Manchester Diabetes Centre, Manchester Royal Infirmary, Manchester, UK. Participants will attend the Manchester Clinical Research Facility (MCRF), Manchester, on two occasions. In random order, they will undergo two closed-loop study days using either faster-acting insulin aspart or insulin aspart. During the study days, the closed-loop control algorithm will automatically modulate d insulin infusion rate based on real-time subcutaneous glucose sensor measurements. Participants will receive standardised meals with half usual meal bolus for the evening meal and no meal bolus for lunch time meal during each study day.

Registry
clinicaltrials.gov
Start Date
December 23, 2020
End Date
August 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The subject is 18 years and older
  • The subject has type 1 diabetes, as defined by WHO for at least 1 year or is confirmed C-peptide negative
  • The subject will have been an insulin pump user for at least 3 months
  • The subject is treated with any of the rapid acting insulin analogues
  • The subject is willing to adhere to study procedures
  • HbA1c ≥ 7.0% (53 mmol/mol) and ≤ 10 % (86mmol/mol) based on analysis from local laboratory or equivalent within 3 months prior to enrolment
  • The subject is literate in English

Exclusion Criteria

  • Non-type 1 diabetes mellitus including those secondary to chronic disease
  • Any other physical or psychological disease likely to interfere with the normal conduct of the study
  • Untreated celiac disease or hypothyroidism
  • Current treatment with drugs known to interfere with glucose metabolism, e.g. systemic corticosteroids, Metformin, SGLT2 inhibitors, non-selective beta-blockers and MAO inhibitors etc.
  • Known or suspected allergy against insulin
  • Subjects with clinical significant nephropathy, neuropathy or proliferative retinopathy as judged by the investigator
  • Total daily insulin dose \> 2 U/kg/day
  • Total daily insulin dose \< 10 U/day
  • Pregnancy, planned pregnancy, or breast feeding

Outcomes

Primary Outcomes

Time spent in the target glucose range

Time Frame: 23 hours

Time spent in the target glucose range between 3.9 to 10.0 mmol/l (70 to 180mg/dl) based on sensor glucose levels between the hours of 19:00 on day 1 and 18:00 hours on day 2 of the inpatient stay.

Secondary Outcomes

  • Time spent in the target glucose range within 4 hours of each meal(4 hours)
  • The time with sensor glucose levels <3.0 (54mg/dl)(23 hours)
  • AUC of glucose below 3.0mmol/l (54mg/dl)(23 hours)
  • Incremental area under the curve of sensor glucose level within 4 hours of each meal(4 hours)
  • Time spent below target glucose(23 hours)
  • Time spent above target glucose(23 hours)
  • Average, coefficient of variation and standard deviation glucose levels(23 hours)
  • The time with sensor glucose levels < 3.5 mmol/l (63 mg/dl)(23 hours)
  • The time with sensor glucose levels <2.8 mmol/l (50 mg/dl)(23 hours)
  • The time with sensor glucose levels in the significant hyperglycaemia(23 hours)
  • Total, basal and bolus insulin dose(23 hours)

Study Sites (1)

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