Closed Loop From Onset in Type 1 Diabetes

Diabetes Mellitus Clinical Trial

— CLOuD  

Official title:

An Open-label, Multicentre, Randomised, Single-period, Parallel Design Study to Assess the Effect of Closed Loop Insulin Delivery From Onset of Type 1 Diabetes in Youth on Residual Beta Cell Function Compared to Standard Insulin Therapy

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02871089
• Other study ID #: CLOuD
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 2017
• Est. completion date: July 31, 2024

Study information

• Verified date: May 2024
• Source: University of Cambridge
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to use a novel treatment approach, the artificial pancreas, after diagnosis of type 1 diabetes (T1D) to improve glucose control with the anticipated improvements of residual C-peptide secretion.

This is an open-label, multicentre, single-period, randomised, parallel group design study. It is expected that a total of up to 190 subjects (aiming for 96 randomised subjects) will be recruited within ten working days of diagnosis of type 1 diabetes through paediatric diabetes centres in the UK. Half of the participants aged 10 to 16.9 years will be treated by conventional insulin injections and the other half by the artificial pancreas (closed loop insulin delivery system). Each treatment will last 24 months. All participants completing the 24 month study period will be invited to continue in an optional extension phase with the treatment allocated at randomisation for a further 24 months.

Subjects in the intervention group will receive additional training on components of the artificial pancreas, i.e. insulin pump and continuous glucose monitoring (CGM), prior to starting closed loop insulin delivery. Subjects in the control intervention group will continue with standard therapy, i.e. multiple daily injection therapy. The study includes up to 14 visits and 1 telephone/email contact for subjects completing the study. After run-in and randomisation, visits will be conducted every 3 months in both arms. Beta-cell function will be assessed by serial measurement of C-peptide in response to a standardised mixed meal tolerance test (MMTT). MMTTs will be conducted at baseline, 6-,12- and 24 months post diagnosis.

The primary outcome is the between group difference in the area under the stimulated C-peptide curve (AUC) of the MMTT at 12 month post diagnosis. Secondary outcomes include between group differences in stimulated C-peptide AUC over 24 months, differences in glycaemic control as assessed by HbA1c, time spent in glucose target range, glucose variability, hypo- and hyperglycaemia as recorded by periodically applied CGM, as well as insulin requirements and change in bodyweight. Additionally, cognitive, emotional and behavioural characteristics of participating subjects and parents will be assessed, and a cost utility analysis on the benefits of closed loop insulin delivery will be performed. Safety evaluation comprises assessment of the frequency of severe hypoglycaemic episodes, diabetic ketoacidosis (DKA) and number, nature and severity of other adverse events.

Description:

Purpose of the study:

• To determine whether continued intensive metabolic control using closed loop insulin delivery (CL) following diagnosis of type 1 diabetes can preserve C-peptide secretion as a marker of residual beta cell function compared to standard multiple daily injections (MDI) therapy

Primary objective:

• To assess residual C-peptide secretion 12 months after diagnosis of type 1 diabetes in participants receiving either CL insulin delivery or standard MDI therapy

Secondary Objectives:

• Biochemical:

• To compare effects of study interventions on residual C-peptide secretion over 24 months following diagnosis

• To examine how intensive diabetes management using CL insulin delivery affects glucose control in terms of safety and efficacy over 24 months

• Human Factors: To assess cognitive, emotional, and behavioural characteristics of participating subjects and family members and their response to closed loop insulin delivery and clinical trial

• Health economics: To perform cost utility analysis and inform reimbursement decision-making

Study design:

• An open-label, multi-centre, randomised, single period, two-arm parallel group study with internal pilot, contrasting closed loop with MDI with an optional 24 month extension phase.

Sample Size:

• 96 participants randomised (48 per group); each clinical site will aim to recruit between 15 and 20 participants

Maximum duration of study for a subject:

• 24 months (48 months if opting to participate in extension phase)

Recruitment:

• Recruitment will take place at Addenbrooke's Hospital, Cambridge, Leeds Teaching Hospital, Leeds, Alder Hey Children's Hospital, Liverpool, Nottingham Hospital, Nottingham, Oxford Children's Hospital, Oxford, Southampton Children's Hospital, Southampton and Royal Hospital for Sick Children, Edinburgh..

Consent

• Written consent/assent will be obtained from participants and/or guardians according to Research Ethics Committee (REC) requirements.

Screening and baseline assessment:

Eligible participants will undergo a screening evaluation including the following activities:

• medical (diabetes) history

• body weight, height and blood pressure measurement

• record of current insulin therapy

• screening and baseline blood sampling

During a baseline visit, the following assessments/ interventions will be carried out at the clinical research facility:

• mixed meal tolerance test (MMTT)

• blood sampling for lipid profile

• centrally measured HbA1c and subsequent immunological analyses

• questionnaires

• computerised cognitive testing

• initiating blinded CGM to assess baseline glycaemic control

Run in period:

• Following consent/screening and baseline assessment, multiple daily injection therapy will be continued in all participants. All participants will receive non study related core diabetes training as per usual clinical practice for a period of up to three weeks.

• All subjects will be provided with 24 hour telephone helpline and will also be given written instructions about when to contact clinical team.

Randomisation:

• Eligible participants will be randomised in a 1:1 ratio using central randomisation software to either closed loop or standard therapy i.e. MDI.

1. Closed loop (interventional arm) Following randomisation, participants in the closed loop group will receive additional training sessions to cover key aspects of insulin pump use and CGM, prior to starting closed loop insulin delivery.

Once competent in the use of the study pump and CGM system, participants will receive training required for safe and effective use of the closed loop system. During a 2-4 hour session participants will operate the system under the supervision of the clinical team. Competency on the use of closed loop system will be evaluated. Thereafter, participants are expected to use closed loop for 24 months without supervision or remote monitoring. The 24 hour support helpline will be available in case of problems.

2. Multiple daily injections (control arm) Participants in the control group will receive additional training sessions following randomisation including a refresher on carbohydrate counting skills, and insulin dose adjustments.

Standard therapy (i.e. MDI) will be applied for 24 months. Participants will be allowed to switch to insulin pump therapy if clinically indicated.

Follow up assessments (3-, 6-, 9-, 12-, 15-, 18-, 21- months):

• Follow up study visits will be conducted 3 monthly including data downloads/recording of insulin requirements, adverse event recording, and blood sampling (HbA1c).

• Participants will be fitted with blinded CGM systems at the end of each follow up visit. The sensors will be worn at home for up to 14 days and will be sent back to the research team.

• MMTTs will be performed at 6 month and 12 month follow up visit.

• Sleep will be assessed using a wristwatch device for 7 days following study visits at 6 and 12 months post diagnosis. Concomitantly, a sleep diary and sleep quality questionnaire will be distributed.

• Validated questionnaires evaluating the impact of the technology on quality of life, life change, diabetes management and fear of hypoglycaemia will be completed at the 12 month visit.

• At 12 months, participants will repeat the computerised cognitive tests first administered at baseline.

• Qualitative interviews will be conducted at month 12 in a subset of subjects and parents int he closed-loop arm.

End of study assessments (24 months):

• A MMTT will be performed.

• A blood sample will be taken for measurement of HbA1c, lipids and immunological analyses.

• Validated questionnaires evaluating the impact of the technology on quality of life, life change, diabetes management and fear of hypoglycaemia will be completed.

• Participants will repeat the computerised cognitive tests first administered at baseline.

• Sleep will be assessed using a wristwatch device for 7 days within the last month of the trial. Concomitantly, a sleep diary and sleep quality questionnaire will be distributed.

• Participants and families will be invited to attend focus group discussions. 24-hour telephone helpline:

• In case of any technical device or problems related to diabetes management such as hypo- or hyperglycaemia, subjects will be able to contact a 24-hour telephone helpline to the local clinical and research team at any time. The local research team will have access to central 24 hour advice on technical issues.

Procedures for safety monitoring during trial:

• Standard operating procedures for monitoring and reporting of all adverse events (AE) will be in place, including serious adverse events (SAE), serious adverse device effects (SADE) and specific adverse events such as severe hypoglycaemia.

• Subjects will be asked to test and record blood or urine ketones if their finger prick glucose is above 14.0 mmol/l, as part of the safety assessment for hyperglycaemia.

• A data monitoring and ethics committee (DMEC) will be informed of all serious adverse events and any unanticipated serious adverse device effects that occur during the study and will review compiled adverse event data at periodic intervals.

Criteria for withdrawal of patients on safety grounds:

• A subject, parent, or guardian may terminate participation in the study at any time without necessarily giving a reason and without any personal disadvantage. An investigator can stop the participation of a subject after consideration of the benefit/risk ratio. Possible reasons are:

1. Serious adverse events

2. Significant protocol violation or non-compliance

3. Failure to satisfy competency assessment

4. Decision by the investigator, or the Sponsor, that termination is in the subject's best medical interest

5. Pregnancy, planned pregnancy, or breast feeding

6. Allergic reaction to insulin Efforts will be made to retain subjects in follow up for the final primary outcome assessment even if the intervention is discontinued, unless the investigator believes that it will be harmful for the subject to continue in the trial.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 96
• Est. completion date: July 31, 2024
• Est. primary completion date: July 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 10 Years to 16 Years

Eligibility

Inclusion Criteria:

1. Diagnosis of type 1 diabetes within previous 21 days. Day 1 will be defined as the day insulin was first administered. Type 1 diabetes will be defined according to WHO criteria using standard diagnostic practice.

[WHO definition: 'The aetiological type named type 1 encompasses the majority of cases with are primarily due to beta-cell destruction, and are prone to ketoacidosis. Type 1 includes those cases attributable to an autoimmune process, as well as those with beta-cell destruction for which neither an aetiology nor a pathogenesis is known (idiopathic). It does not include those forms of beta-cell destruction or failure to which specific causes can be assigned (e.g. cystic fibrosis, mitochondrial defects, etc.).']

2. The subject is at least 10 years and not older than 16.9 years

3. The subject/carer is willing to perform regular capillary blood glucose monitoring, with at least 4 blood glucose measurements taken every day

4. The subject is literate in English

5. The subject is willing to wear glucose sensor

6. The subject is willing to wear closed loop system at home

7. The subject is willing to follow study specific instructions

8. The subject is willing to upload pump and CGM data at regular intervals

Exclusion Criteria:

1. Physical or psychological condition likely to interfere with the normal conduct of the study and interpretation of the study results as judged by the investigator

2. Current treatment with drugs known to interfere with glucose metabolism, e.g. systemic corticosteroids, non-selective beta-blockers and MAO inhibitors etc.

3. Known or suspected allergy to insulin

4. Regular use of acetaminophen

5. Lack of reliable telephone facility for contact

6. Pregnancy, planned pregnancy, or breast feeding

7. Living alone

8. Severe visual impairment

9. Severe hearing impairment

10. Medically documented allergy towards the adhesive (glue) of plasters or unable to tolerate tape adhesive in the area of sensor placement

11. Serious skin diseases (e.g. psoriasis vulgaris, bacterial skin diseases) located at places of the body, which potentially are possible to be used for localisation of the glucose sensor

12. Illicit drugs abuse

13. Prescription drugs abuse

14. Alcohol abuse

15. Sickle cell disease, haemoglobinopathy, receiving red blood cell transfusion or erythropoietin within 3 months prior to time of screening

16. Eating disorder such as anorexia or bulimia

17. Milk protein allergy

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1
• Type 1 Diabetes

Intervention

Device:
• Closed-loop system (Florence M or CamAPS FX)
The automated closed-loop system (FlorenceM) will consist of: Sensor augmented Medtronic insulin pump 640G (Medtronic Minimed, CA, USA) incorporating the Medtronic Enlite/Guardian 3 real time CGM and glucose suspend feature. An Android smartphone containing the Cambridge model predictive algorithm and communicating wirelessly with the insulin pump using a proprietary translator device. The automated closed-loop system (CamAPS FX) will consist of: Dana R or RS insulin pump Dexcom G6 real-time CGM CamAPS FX App on an unlocked android smartphone. Rapid acting insulin analogue will be used (insulin aspart, insulin lispro, insulin glulisine or similar or ultra-rapid insulin analogue).

Other:
• Multiple Daily Injections
Rapid acting insulin analogue and long acting insulin analogue will be subcutaneously administered using CE-marked insulin pen devices in accordance with the manufacturer's instructions for their intended purposes. Participants will be given long acting analogue (insulin glargine, insulin detemir or similar) once or twice daily according to their needs and boluses of rapid acting analogue (insulin aspart, insulin lispro, insulin glulisine or similar or ultra-rapid insulin analogue) when carbohydrates are consumed.

Locations

Country	Name	City	State
United Kingdom	Cambridge University Hospitals NHS Foundation Trust	Cambridge
United Kingdom	Royal Hospital for Sick Children	Edinburgh
United Kingdom	St James's University Hospital	Leeds	West Yorkshire
United Kingdom	Alder Hey Children's NHS Foundation Trust	Liverpool	West Derby
United Kingdom	Nottingham Children's Hospital	Nottingham	Nottinghamshire
United Kingdom	John Radcliffe Hospital	Oxford	Oxfordshire
United Kingdom	Southampton Children's Hospital	Southampton	Hampshire

Sponsors (9)

Lead Sponsor	Collaborator
University of Cambridge	Alder Hey Children's NHS Foundation Trust, Cambridge University Hospitals NHS Foundation Trust, Jaeb Center for Health Research, Nottingham University Hospitals NHS Trust, Oxford University Hospitals NHS Trust, The Leeds Teaching Hospitals NHS Trust, University Hospital Southampton NHS Foundation Trust, University of Edinburgh

Country where clinical trial is conducted

United Kingdom, 

References & Publications (3)

Hovorka R. Artificial Pancreas Project at Cambridge 2013. Diabet Med. 2015 Aug;32(8):987-92. doi: 10.1111/dme.12766. Epub 2015 Apr 15. — View Citation

Tauschmann M, Allen JM, Wilinska ME, Thabit H, Stewart Z, Cheng P, Kollman C, Acerini CL, Dunger DB, Hovorka R. Day-and-Night Hybrid Closed-Loop Insulin Delivery in Adolescents With Type 1 Diabetes: A Free-Living, Randomized Clinical Trial. Diabetes Care. 2016 Jul;39(7):1168-74. doi: 10.2337/dc15-2078. Epub 2016 Jan 6. — View Citation

Thabit H, Tauschmann M, Allen JM, Leelarathna L, Hartnell S, Wilinska ME, Acerini CL, Dellweg S, Benesch C, Heinemann L, Mader JK, Holzer M, Kojzar H, Exall J, Yong J, Pichierri J, Barnard KD, Kollman C, Cheng P, Hindmarsh PC, Campbell FM, Arnolds S, Pieber TR, Evans ML, Dunger DB, Hovorka R. Home Use of an Artificial Beta Cell in Type 1 Diabetes. N Engl J Med. 2015 Nov 26;373(22):2129-2140. doi: 10.1056/NEJMoa1509351. Epub 2015 Sep 17. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Severe hypoglycaemic episodes	Frequency of severe hypoglycaemic episodes	24 month intervention period
Other	Diabetes ketoacidosis	Frequency of severe diabetes ketoacidosis	24 month intervention period
Other	Adverse Events	Number, nature and severity of other adverse events. The period during which adverse events will be reported is defined as the period from the beginning of the study (obtaining informed consent) until 3 weeks after the end of the study participation	24 month intervention period + 3 weeks
Other	Serious Adverse Events	Number, nature and severity of serious adverse events. The period during which adverse events will be reported is defined as the period from the beginning of the study (obtaining informed consent) until 3 weeks after the end of the study participation	24 month intervention period + 3 weeks
Other	Assessment of the frequency of use of the closed loop system	Utility evaluation	24 month intervention period
Other	Assessment of the duration of use of the closed loop system.	Utility evaluation	24 month intervention period
Other	Cognitive Assessment	Assessment of cognitive changes using computerized cognitive testing.	Baseline, 6, 12 and 24 months post diagnosis
Other	Health Economic Evaluation	Cost utility analysis using the CORE Diabetes Model (CDM; IMS Health, Basel, Switzerland) on the benefits of closed loop insulin delivery to inform reimbursement decision-making.	24 month intervention period
Other	Quantitative Human Factor Assessment	Questionnaires will be completed by participants and parents/guardians.	Baseline,12 and 24 months post diagnosis
Other	Qualitative Human Factor Assessment	Interview and focus group with participants and parents/guardians.	12 and 24 months post diagnosis
Primary	Area under the meal stimulated C-peptide curve (AUC) during a mixed meal tolerance test (MMTT)		12 months post diagnosis
Secondary	Mean stimulated C-peptide AUC during a mixed meal tolerance test		Baseline, 6 months and 24 months post diagnosis
Secondary	HbA1c Levels	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Percentage of patients in each group with HbA1c <7.5% (58mmol/mol)	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Percentage of time spent with sensor glucose readings in the target range (3.9 to 10mmol/l)	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Mean sensor glucose level	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Standard deviation of sensor glucose levels	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Coefficient of variation of sensor levels	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Percentage of time with sensor glucose levels <3.5 mmol/l and <2.8 mmol/l	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Percentage of time spent below target glucose (3.9mmol/l)	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	AUC of sensor glucose below 3.5mmol/l	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Time spent with sensor glucose above target (10.0 mmol/l)	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Time with sensor glucose levels in significant hyperglycaemia (glucose levels > 16.7 mmol/l)	Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Insulin Requirements	Total, basal and bolus insulin dose (U/kg). Both arms	Baseline, 3, 6, 9, 12, 15, 18, 21 and 24 months post diagnosis
Secondary	Weight	Change in body mass index (BMI) standard deviation score. Both arms	Baseline, 6, 12 and 24 months post diagnosis
Secondary	Blood pressure	Both arms	Baseline, 6, 12 and 24 months post diagnosis
Secondary	Lipid profile	Both arms	Baseline, 12 and 24 months post diagnosis