Feasibility of ECG-Based Glucose Monitoring System
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: No intervention.
- Who it may be relevant to
- Registry conditions: Diabetes Mellitus. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Taiwan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Feasibility Assessment of Novel ECG-Based Continuous Glucose Monitoring System
Overview
This is a single-center, open-label clinical trial to assess the feasibility of using ECG information in estimating glucose level continuously in adult subjects.
Detailed description
About 165 subjects distributed in 3 categories according to the risk of developing events of hyperglycemia or hypoglycemia will be enrolled. Subjects will wear a portable ECG recorder to monitor ECG information and use 3 blood glucose monitoring methods to monitor blood glucose level over time. All data will be pooled together to train a specific artificial intelligence (AI) algorithm to conduct a blood glucose detection model using ECG features. The trial period is about 21 days.
Interventions
- Other No intervention
No intervention is conducted in this study.
Primary outcome measures
- To assess the accuracy of glucose level determined by the glucose detection model through ECG data and blood glucose monitoring values. [Time frame: 14 days]
Eligibility criteria
Inclusion criteria
- Males and females, age 18 years or older.
- Subjects can communicate clearly, fully understand the informed consent form, and are aware of the rights and obligations of the study.
- Category 1: Subjects without a medical history of hyperglycemia / hypoglycemia or type 1 / type 2 diabetes.
Category 2: Subjects having diabetes mellitus (DM) and HbA1c value of. 5.5% to 10%, with eGFR ≥ 60 mL/min.
Category 3: Subjects having chronic kidney disease (CKD) and diabetes. mellitus (DM), with eGFR < 60 mL/min.
- Willing and able to participate in all aspects of the study.
Exclusion criteria
- Subjects suffering from insomnia or severe digestive system disorders within 3 months prior to the screening visit.
- Subjects who are addicted to alcohol or caffeine.
- Existing severe cardiac conditions such as recent myocardial infarction or advanced heart failure within 6 months prior to the screening visit.
- Has experienced an episode of confirmed or suspected diabetic ketoacidosis (DKA) within 6 months prior to the screening visit.
- Subjects who are vulnerable groups or with higher risks, such as HIV carriers, pregnant women or planning to become pregnant within the study duration, breast-feeding mothers, subjects with rare diseases, physical disabilities, incurable fatal diseases, dependents in nursing homes, incapacity, or intellectual or mental disabilities.
- Has a concomitant disease or condition that may compromise subject safety such as unstable coronary heart disease, cystic fibrosis, serious psychiatric disorder, or any other uncontrolled medical conditions.
- Any active infection or malignancy requiring acute therapy.
- Having coagulation disorders.
- Has known allergy to medical adhesives.
- Subjects using any cardiac related implantable medical devices such as a pacemaker and so on.
- Subjects on certain drugs known to cause arrhythmias or significantly impact kidney function or blood glucose levels (except for the current daily use medication).
- Subjects have used defibrillators within 3 months prior to the screening visit.
- Currently participating in another device or drug study.
- Currently receiving dialysis treatment or planning to receive dialysis during the study.
- Any other clinical condition that, in the investigator's judgment, would potentially compromise study compliance or the ability to evaluate safety/efficacy.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Taiwan · 1 center
- Landseed International Hospital — Taoyuan
Identifiers
NCT: NCT06883682 · SWM-BG-001