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Accuracy of Continuous Glucose Monitoring in Critically Ill Patients

Accuracy of Continuous Glucose Monitoring in Critically Ill Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042036
Enrollment
Unknown
Registered
2021-01-12
Start date
2021-01-05
Completion date
Unknown
Last updated
2021-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus

Interventions

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. The length of stay in ICU was more than 72 hours; 3. APACHE-II score (acute physiology and chronic health score) >= 15; 4. Good venous access, evaluated by researchers or appropriate staff; 5. The subjects are willing to follow the research procedures and conduct research visits; 6. No other clinical trials were conducted within 3 months; 7. The subjects were willing to receive IV glucose test 4 times per hour for 7 hours.

Exclusion criteria

Exclusion criteria: 1. Patients using hormone and immunosuppressant; 2. Patients with pregnancy or planned pregnancy; 3. Patients with severe anemia (hemoglobin < 6G / dl); 4. Allergic to the adhesive used in the instrument; 5. There were adverse skin diseases (such as cowhide moss, rash, etc.) in the instrument placement area; 6. Patients who need MRI examination; 7. Refused to sign informed consent.

Design outcomes

Primary

MeasureTime frame
The consistency of venous blood glucose and blood glucose measured by scanning glucose monitoring system;SEN, SPE, ACC, AUC of ROC;

Countries

China

Contacts

Public ContactWeifeng Huang

Shanghai Sixth People's Hospital

breeze-huang@hotmail.com+86 18930173670

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026