CGM in Icodextrin PD

Elaine Chow

Status: Not yet enrolling

Conditions: Dialysis; Diabetes Mellitus (Diagnosis); Continuous Glucose Monitoring; End Stage Renal Disease (ESRD)

Treatments: Device: Continuous glucose monitoring system

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT06838819

IcoSimplera

Details and patient eligibility

About

Assessment of performance (precision and accuracy) of Simplera™ CGM as compared with a gold standard reference laboratory method (YSI glucose) in diabetes patients on peritoneal dialysis with icodextrin

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Type 1 or 2 diabetes mellitus for at least 3 months
2. On continuous ambulatory peritoneal dialysis (CAPD) or APD for at least 2 months
3. On icodextrin PD solutions for at least 1 month or planned for switching to icodextrin PD solutions within 3 months of screening
4. Male or female age ≥ 18 years old and ≤ 75 year old.
5. Women who are not pregnant, lactating or planning a pregnancy during their participation in the clinical study.
6. Willingness, ability and commitment to comply with the testing, procedure and follow-up outlined in this protocol including (but not limited to) frequency of clinic visits and use of pre-specified glucose monitoring devices.
7. Willingness to abstain from swimming during their participation in the measurement phase.
8. In the opinion of the investigator, absence of any physical limitations, addictive diseases, or underlying medical conditions (including mental health) that may preclude the patient from being a good study candidate.
9. Written informed consent to participate in the study provided by the patient.

Exclusion criteria

1. Poorly controlled diabetes mellitus with HbA1c>11%
2. Peritonitis within 1 month of screening
3. Planned for switching to hemodialysis or living donor transplant in the future 1 month
4. Currently pregnant, as demonstrated by a positive pregnancy test at screening for women of reproductive potential
5. Any active acute or chronic disease or condition that, in the opinion of the investigator, might interfere with the performance of this study.
6. Any active acute or chronic infectious disease that, in the opinion of the investigator, would pose an excessive risk to study staff.
7. Current use or recent exposure to any medication that in the opinion of the investigator could have an influence on the patient's ability to participate in this study or on the performance of the test device.
8. Extensive skin changes/diseases that preclude wearing the required number of devices on normal skin at the proposed application sites (e.g., extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis).
9. Have a known allergy to medical-grade adhesives, or known hypersensitivity to any of the products used in the study.
10. Blood donation of more than 500 ml within the last three months
11. Currently participating in another investigational study protocol where the testing or results may interfere with study compliance, diagnostic results, or data collection.
12. Has a MRI scan, CT scan, or diathermy scheduled during the proposed study participation.
13. An identified protected vulnerable patient (including but not limited to those in detention, or a prisoner).
14. Women of reproductive potential who are unwilling to adopt contraceptive measures during the study period
15. Patients with history of pacemaker and prosthesis implantation.
16. Continuous use of real-time CGM for personal diabetes management in the three months prior to screening (sensor use >80% of time)