RecruitingNot ApplicableNCT06579404

Closed-loop in Adults With Type 2 Diabetes

An Open-label, Multinational, Multicentre, Randomised, Single-period Parallel Study to Assess the Efficacy, Safety and Utility of Fully Closed-loop Insulin Delivery Compared to Standard Insulin Therapy With CGM in Adults With Type 2 Diabetes


Sponsor

University of Cambridge

Enrollment

224 participants

Start Date

Dec 6, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The main objective of this study is to determine the efficacy, safety and utility of fully closed-loop glucose control in the home setting in adults with type 2 diabetes (T2D). This study builds on previous and on-going studies of closed-loop systems that have been performed in Cambridge in adults with type 2 diabetes in the inpatient and in the home setting and in children and adults with type 1 diabetes. This is an open-label, multi-national, multi-centre, randomised, single-period parallel study, involving a run-in period followed by a 26-week intervention period during which glucose levels will be controlled either by a fully closed-loop system or by participants usual insulin therapy with continuous glucose monitoring. A total of up to 224 adults with type 2 diabetes using insulin will be recruited through outpatient diabetes clinics, primary care centres, social media advertising and other established methods at participating centres. Participants will receive appropriate training in the safe use of the study devices. The primary outcome is the between group difference in HbA1c at 26 weeks. Other key outcomes include the time spent with glucose levels within, above and below the target glucose range (3.9-10.0mmol/L) and mean sensor glucose as recorded by CGM over the 26 weeks. Insulin requirements, body weight, renal and liver function will also be compared. Safety evaluation comprises severe hypoglycaemic episodes, and other adverse and serious adverse events. Human factors outcomes include CGM \& closed-loop usage, questionnaires and semi-structured interviews.


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • Aged 18 years and older
  • Type 2 diabetes diagnosed for at least 12 months
  • Established on an SGLT2 inhibitor and/or GLP-1 receptor agonist for at least 3 months, or have been offered these therapies previously.
  • Treatment with insulin therapy for at least 6 months
  • HbA1c ≤ 15% (140 mmol/mol) analysis from local laboratory or equivalent
  • Willing to wear study devices and follow study instructions
  • Capacity to consent to participate in the study

Exclusion Criteria14

  • Type 1 diabetes
  • Current use of insulin pump
  • Current use of any closed-loop system
  • Any physical/psychological disease or medication(s) likely to interfere with the conduct of the study and interpretation of the study results, as judged by study clinician
  • Known or suspected allergy against insulin
  • Medically documented allergy towards the adhesive
  • Pregnancy, planned pregnancy, or breast feeding
  • Severe visual impairment
  • Severe hearing impairment
  • Medically documented allergy towards the adhesive (glue) of plasters
  • Serious skin diseases located at places of the body, which potentially are possible to be used for localisation of the glucose sensor
  • Illicit drugs abuse
  • Prescription drugs abuse
  • Alcohol abuse

Interventions

DEVICECamAPS HX

The automated closed loop system (CamAPS HX) will consist of: YpsoPump insulin pump Freestyle Libre 3 glucose sensor Smartphone hosting CamAPS HX app with the Cambridge model predictive control algorithm

OTHERStandard insulin therapy with glucose sensor

Participants usual insulin therapy with Freestyle Libre 3 glucose sensor


Locations(12)

University of Melbourne

Melbourne, Australia

Medical University of Graz

Graz, Austria

Diabetes Centre, Institute of Clinical and Experimental Medicine

Prague, Czechia

CHU de Toulouse

Toulouse, France

Bern University Hospital

Bern, Switzerland

Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust

Cambridge, United Kingdom

Royal Derby Hospital

Derby, United Kingdom

Leicester Diabetes Centre

Leicester, United Kingdom

Guy's and St Thomas' NHS Foundation Trust

London, United Kingdom

King's College Hospital, King's College NHS Foundation Trust

London, United Kingdom

Manchester Royal Infirmary, Central Manchester University Hospitals NHS Foundation Trust

Manchester, United Kingdom

Norfolk and Norwich University Hospital

Norwich, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06579404


Related Trials