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Closing the Loop in Young Children With Type 1 Diabetes

Primary Purpose

Type 1 Diabetes

Status
Unknown status
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Overnight closed-loop insulin delivery
Sponsored by
Daniela Elleri
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes

Eligibility Criteria

2 Years - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The subject is between 2 and 6 years of age (inclusive)
  • The subject has had type 1 diabetes, as defined by WHO criteria for at least 6 months
  • The subject will be an insulin pump user and carers will have a good knowledge of insulin dose adjustment
  • HbA1c below 12 % (108mmol/mol)

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 and interpretation of the study results
  • Current treatment with drugs known to interfere with glucose metabolism such as systemic corticosteroids
  • Known or suspected allergy against insulin

Sites / Locations

  • Wellcome Trust Clinical Research Facility, Addenbrooke's hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Closed-loop with diluted insulin

Closed-loop with non-diluted insulin

Arm Description

Insulin pump therapy using diluted insulin (20 IU/ml) will be driven by computer-based algorithm from 1700 on Day 1 until 0800 on Day 2

Insulin pump therapy using standard non-diluted insulin (100 IU/ml) will be driven by computer-based algorithm from 1700 on Day 1 until 0800 on Day 2

Outcomes

Primary Outcome Measures

Time in target
Time spent with plasma glucose concentration in the target range (3.9-8.0mmol/L)

Secondary Outcome Measures

Time below target
• Time spent with plasma glucose concentration below the target range (<3.9mmol/L)
Glucose variability
• Glucose variability as measured by standard deviation of glucose

Full Information

First Posted
March 14, 2012
Last Updated
April 1, 2013
Sponsor
Daniela Elleri
Collaborators
Cambridge University Hospitals NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT01557634
Brief Title
Closing the Loop in Young Children With Type 1 Diabetes
Official Title
An Open-label, Single-centre, Randomised, 2-period Cross-over Study to Assess the Efficacy and Safety of Overnight Closed-loop Insulin Delivery Using Diluted Insulin in Comparison With Closed-loop With Non-diluted Insulin in Children With Type 1 Diabetes Aged 2 to 6 Years
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Unknown status
Study Start Date
December 2012 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Daniela Elleri
Collaborators
Cambridge University Hospitals NHS Foundation Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The incidence of type 1 diabetes (T1D) is increasing worldwide with evidence of most rapid increase in preschool children. Intensive control of blood glucose levels, although essential to protect against onset and progression of diabetes-related complications, faces unique challenges in toddlers and preschool children. A closed-loop system can enhance accuracy of insulin delivery and help people with T1D attain a tight glucose control avoiding the risk of hypoglycaemia. The main components of the system are a continuous glucose monitor (CGM), an insulin pump and a computer-based 'model predictive algorithm', which calculates the amount of insulin to be given by the insulin pump according to the CGM values. In the studies performed thus far the efficacy and safety of closed-loop glucose control were evaluated in children and adolescents aged 6 to 18 years. The results showed that closed-loop improved control of blood glucose and prevented nocturnal hypoglycaemia, as compared to the conventional insulin pump therapy. The objective of the current study is to extend the evaluation of closed-loop further to younger children aged 2 to 6 years, who may gain a great benefit from this novel therapy. The present study adopts an open-label, randomised, 2 period cross-over design whereby closed-loop insulin therapy using diluted insulin (20IU/ml)will be compared with closed-loop with standard insulin (100IU/ml)in 12 young children with T1D. Participants aged 2 to 6 years will be randomised for two overnight studies in a clinical research facility, during which glucose levels will be controlled by either the computer-based closed-loop algorithm using diluted insulin or by closed-loop with standard insulin. On both occasions, participants will receive a self-selected evening meal and closed-loop will run from 17:00 until 08:00am the following day. The study will take place at the Wellcome Trust Clinical Research Facility, Cambridge with participants recruited from paediatric diabetes clinics in England.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Closed-loop with diluted insulin
Arm Type
Experimental
Arm Description
Insulin pump therapy using diluted insulin (20 IU/ml) will be driven by computer-based algorithm from 1700 on Day 1 until 0800 on Day 2
Arm Title
Closed-loop with non-diluted insulin
Arm Type
Active Comparator
Arm Description
Insulin pump therapy using standard non-diluted insulin (100 IU/ml) will be driven by computer-based algorithm from 1700 on Day 1 until 0800 on Day 2
Intervention Type
Procedure
Intervention Name(s)
Overnight closed-loop insulin delivery
Intervention Description
Basal insulin infusion rates on insulin pump will be directed by MPC algorithm using diluted versus non-diluted insulin
Primary Outcome Measure Information:
Title
Time in target
Description
Time spent with plasma glucose concentration in the target range (3.9-8.0mmol/L)
Time Frame
Between 21:00 on Day 1 and 8:00 on Day 2
Secondary Outcome Measure Information:
Title
Time below target
Description
• Time spent with plasma glucose concentration below the target range (<3.9mmol/L)
Time Frame
Between 21:00 on Day 1 and 8:00 on Day 2
Title
Glucose variability
Description
• Glucose variability as measured by standard deviation of glucose
Time Frame
Between 21:00 on Day 1 and 08:00 on Day 2

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The subject is between 2 and 6 years of age (inclusive) The subject has had type 1 diabetes, as defined by WHO criteria for at least 6 months The subject will be an insulin pump user and carers will have a good knowledge of insulin dose adjustment HbA1c below 12 % (108mmol/mol) 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 and interpretation of the study results Current treatment with drugs known to interfere with glucose metabolism such as systemic corticosteroids Known or suspected allergy against insulin
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daniela Elleri, MD
Phone
+44 1223 7969069
Email
de250@medschl.cam.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roman Hovorka, PhD
Organizational Affiliation
University of Cambrigde
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wellcome Trust Clinical Research Facility, Addenbrooke's hospital
City
Cambridge
ZIP/Postal Code
CB2 0QQ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Janet Allen, RN
Phone
+44 1223 769064
Email
ja385@medschl.cam.ac.uk
First Name & Middle Initial & Last Name & Degree
Roman Hovorka, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
20138357
Citation
Hovorka R, Allen JM, Elleri D, Chassin LJ, Harris J, Xing D, Kollman C, Hovorka T, Larsen AM, Nodale M, De Palma A, Wilinska ME, Acerini CL, Dunger DB. Manual closed-loop insulin delivery in children and adolescents with type 1 diabetes: a phase 2 randomised crossover trial. Lancet. 2010 Feb 27;375(9716):743-51. doi: 10.1016/S0140-6736(09)61998-X. Epub 2010 Feb 4.
Results Reference
background
PubMed Identifier
25537835
Citation
Ruan Y, Elleri D, Allen JM, Tauschmann M, Wilinska ME, Dunger DB, Hovorka R. Pharmacokinetics of diluted (U20) insulin aspart compared with standard (U100) in children aged 3-6 years with type 1 diabetes during closed-loop insulin delivery: a randomised clinical trial. Diabetologia. 2015 Apr;58(4):687-90. doi: 10.1007/s00125-014-3483-6. Epub 2014 Dec 24.
Results Reference
derived
PubMed Identifier
25512874
Citation
Elleri D, Allen JM, Tauschmann M, El-Khairi R, Benitez-Aguirre P, Acerini CL, Dunger DB, Hovorka R. Feasibility of overnight closed-loop therapy in young children with type 1 diabetes aged 3-6 years: comparison between diluted and standard insulin strength. BMJ Open Diabetes Res Care. 2014 Dec 11;2(1):e000040. doi: 10.1136/bmjdrc-2014-000040. eCollection 2014.
Results Reference
derived

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Closing the Loop in Young Children With Type 1 Diabetes

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