Early Feasibility Evaluation of the myLoop Hybrid-Closed-Loop Insulin Delivery System in Type 1 Diabetes

Not Applicable

Not yet recruiting

• Conditions: Type-1-Diabetes

• Registration Number: NCT07087340
• Lead Sponsor: University of Bern

Brief Summary

The study is investigating the early feasibility of a novel algorithm for a hybrid closed-loop (HCL) insulin delivery system in adult patients with Type 1 diabetes.

Participants will attend a study visit where the myLoop system on a smartphone will manage insulin delivery via an insulin pump, using blood glucose values from a continuous glucose meter. Specialized staff and a remote monitoring system, which is integrated into the myLoop system, will oversee the participants.

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-07
• Study First Submitted: 2025-07-24
• Study First Submitted QC: 2025-07-24
• Last Update Submitted: 2025-07-24
• Study First Posted: 2025-07-28
• Last Update Posted: 2025-07-28
• Study Start: 2025-09-01
• Primary Completion: 2025-12-31
• Study Completion: 2026-02-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

• T1D diagnosis for at least one year.
• Aged between 18 and 65 years old (inclusive).
• Currently using insulin for at least six months.
• Currently using closed-loop insulin therapy for at least three months.
• Willingness to suspend any personal CGM for the duration of the pilot study once the study CGM is in place.
• Willingness not to start any new non-insulin glucose-lowering agent during the study (including metformin/biguanides, incretin agonists [GIP/GLP-1RAs or GLP-1RAs], pramlintide, DPP-4 inhibitors, sulfonylureas, Sodium-glucose cotransporter-2 inhibitors [SGLT2 inhibitors], and nutraceuticals).
• Understanding and willingness to follow the protocol and signed informed consent.

Exclusion Criteria

• An HbA1C ≥10% .
• History of diabetic ketoacidosis (DKA) in the past 12 months.
• History of severe hypoglycaemic event (Level 3): defined as seizure or loss of consciousness in the past 12 months.
• Current uncontrolled chronic diabetic microvascular complications (neuropathy, retinopathy, renal diabetes disease, and diabetic gastroparesis).
• Body Mass Index (BMI) ≤18.5 or ≥ 35 kg m2
• Estimated glomerular filtration rate (eGFR) lab value below 30 mL/min/1.73 m2
• Pregnancy or intent to become pregnant during the study.
• Currently breastfeeding or planning to breastfeed.
• Currently uncontrolled seizure disorder.
• Planned surgery during the study duration.
• Have uncontrolled hypertension (systolic BP above or equal to 160 mmHg and/or diastolic BP above or equal to 100 mmHg). If a participant is on anti-hypertensive therapies, doses must be stable for 30 days before screening. For participants with uncontrolled hypertension at the screening visit, antihypertensive medication may be started or adjusted.*
• Personal history of one of the following cardiovascular conditions: acute myocardial infarction, cerebrovascular accident (stroke), unstable angina, or hospitalization due to congestive heart failure (CHF) in the last three months before the screening.
• Conditions that may increase the risk of induced hypoglycemia such as known coronary artery disease, CHF (Have NYHA Functional Classification III or IV CHF), history of any cardiac disorder or arrhythmia, history of cerebrovascular event, hypoglycemia-induced migraine within the past six months, seizure disorder, syncope, adrenal insufficiency, or neurological disease).
• Cystic fibrosis.
• Uncontrolled thyroid disease as judged by the investigator.
• Have an uncontrolled psychiatric condition such as (major depressive disorder, schizophrenia, bipolar disorder, or other serious mood or anxiety disorder, alcohol or drug abuse).
• Treatment with a non-insulin glucose-lowering agent, except metformin, in stable doses in the last three months.
• Participants receiving or have received systemic glucocorticoid therapy within three months before screening (Prednisolone 10mg daily or equivalent >2 weeks) or chronic systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, single intraarticular injection, or inhaled preparations).
• Have current treatment with (or history of, within 3 months before screening) medications that may affect glucose metabolism, as judged by the investigator.
• Current enrolment in another clinical trial, unless approved by the investigator of both studies, and if the clinical trial is a non-interventional registry trial.
• Have evidence of a significant active, uncontrolled medical condition or a history of any medical problem capable of constituting a risk when using the study devices or interfering with the interpretation of data, as judged by the study physician at screening.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Percentage of time with the system functioning in closed-loop mode	10 hours
Failure rate of the HCL algorithm	10 hours
Failure rate of the communication with CGM device	10 hours
Failure rate of the communication with Insulin pump	10 hours
Failure rate of the user interface (BernSHELL)	10 hours
Failure rate of the web monitoring tool (DigiCARE)	10 hours

Trial Locations

Locations (1)

Inselspital, Universitätsspital; Universitätsklinik für Diabetologie, Endokrinologie, Ernährungsmedizin & Metabolismus (UDEM); 🇨🇭 Bern, Switzerland