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Effect of Real-time Continuous Glucose Monitoring on Glucose Control and Outcomes of Critically Ill Patients

Effect of Real-time Continuous Glucose Monitoring on Glucose Control and Outcomes of Critically Ill Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01992965
Enrollment
144
Registered
2013-11-25
Start date
2014-04-30
Completion date
2016-05-31
Last updated
2014-05-07

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

Conditions

Hyperglycemia

Keywords

continuous glucose monitoring;, critically ill;

Brief summary

The purpose of the study is to evaluate the effect of real-time continuous glucose monitoring system on glucose control and outcomes of critically ill patients.

Detailed description

Real-time continuous glucose monitoring system has shown great accuracy and feasibility in critically ill patients. However, its impact on glucose control and outcomes has nearly unknown. Thus, Investigators designed this study to evaluate the effect of real-time continuous glucose monitoring system on glucose control and outcomes of critically ill patients.

Interventions

OTHERDifferent methods of blood glucose monitoring between groups

Finger prick blood glucose in conventional group versus real-time continuous glucose monitoring system of continuous glucose monitoring group

Sponsors

Kang Yan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* More than 18 years old male or female; * Expected ICU stays longer than 72 hours; * Glucose level more than 8 mmol/L when enrolls in the ICU; * Patients or their legal surrogates have signed the informed consent.

Exclusion criteria

* Pregnant or lactating women; * ICU stays less than 72 hours; * Usage of real-time continuous glucose monitoring system is considered as a contraindication.

Design outcomes

Primary

MeasureTime frame
Glycemic Control Measures including: Percentage of target blood glucose levels (defined as between 8mmol/L and 10mmol/L); Time of hyperglycemia (defined as >10mmol/L); Hypoglycemia rate (defined as < 2.2mmol/L); Glucose lability indexGlycemic control measures will be assessed up to five days.

Secondary

MeasureTime frame
Prognosis Measures including: Duration of mechanical ventilation;Time of ICU stay; Time of hospital stay; 28 days - mortality rateAll the participants will be followed for the duration of hospital stay or 28 days.
CostCost associated with glucose monitoring

Countries

China

Contacts

Primary ContactYan Kang, MD
kang_yan_123@163.com86-028-85422508
Backup ContactYan-yan Zuo, MM
zyyan21@163.com86-028-85422506

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026