Continuous Bloodsugar Monitoring System With a Sensor Compared to Fingerstick Bloodsugar Monitoring
Recruiting now · Not applicable
Conditions studied: Diabetes Mellitus, Hypoglycemia (Diabetic), Hypoglycemia Night, Hyperglycemia
In brief
This clinical trial aims to compare a continuous glucose monitoring system with traditional fingerstick blood glucose monitoring. The study focuses on adult patients in general surgical wards who need regular blood glucose checks due to the risk of low or high blood sugar levels. The goal is to learn if using a continuous glucose monitoring system is better than fingerstick monitoring in managing glucose levels, preventing complications, improving patient satisfaction and experience, reducing nursing staff workload, and improving nursing staff' experience. The study also compares the accuracy of glucose readings from the continuous glucose monitoring system with those from fingerstick tests and blood samples. The hypothesis is that CGMS is accurate and effective for monitoring glucose levels in surgical patients. This could lead to better blood sugar control, fewer complications, shorter hospital stays, and improved experiences for both patients and nursing staff.
Key facts
- Study ID
- NCT06473480
- Run by
- Odense University Hospital
- People needed
- 329
- Starts
- 2024-06-26
- Expected to finish
- 2025-12-31
- Last updated by the study team
- 2025-04-03
Who can join
Age: 18 and older, up to 110. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Hospitalized patients (≥ 18 years old) in surgical wards
- Glucose measurements at least 4 times (OUH) and 3 times (SUH) daily for at least three days, prescribed by surgeon
- Expected hospitalization for at least three days
- Communicates in Danish
- Signed a declaration of consent to study participation
- At risk of hypo- and hyperglycemia (with or without a diabetes diagnosis)
- Specific for substudy 4 inclusion criteria as above with the following add on: Patients being treated with insulin at discharge and patients residing within the OUH admission area.
You may not qualify if…
- Cognitively impaired patients
- Indication for glucose monitoring solely because of parenteral nutrition treatment
- Patients admitted with a CGMS
- Patients from the point-of-care fingerstick capillary glucose monitoring group cannot be included in the continuous glucose monitoring system group
- Eligibility criteria solely for substudy 7
- Inclusion Criteria:
- Nursing staff with at least one month of experience with both point-of-care fingerstick capillary glucose monitoring and continuous glucose monitoring system and are registered nurses or certified nursing assistants
Where it is running
- Department of Surgery, Zealand University Hospital — Køge, Køge, Denmark (enrolling)
- The Department of Surgery, Odense Univeristy Hospital — Odense, Odense, Denmark (enrolling)
Full record on ClinicalTrials.gov
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