Condition: Diabetes Mellitus · Hypoglycemia (Diabetic) · Hypoglycemia Night · Sponsor: Odense University Hospital
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.
This description comes directly from the study's public registry record.
Helen Schultz, RN, PhD · +4522401513 · Helen.Schultz@rsyd.dk
Karoline Schousboe, MD, PhD · +4524349740 · Karoline.Schousboe@rsyd.dk
Always discuss trial participation with your own doctor first.
| Department of Surgery, Zealand University Hospital | Køge, Køge, Denmark | Recruiting |
| The Department of Surgery, Odense Univeristy Hospital | Odense, Odense, Denmark | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06473480