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To discuss an blood glucose control improved protocol for critically ill patients during enteral nutrition

To discuss an blood glucose control improved protocol for critically ill patients during enteral nutrition

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15007517
Enrollment
Unknown
Registered
2015-12-05
Start date
2015-12-05
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hyperglycaemia

Interventions

research group:insulin glargine
contrast group:regular insulin

Sponsors

Beijing Tongren Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients admitted to ICU, anticipated to require intensive care >=2 days, aged >=18 years, continuous infusion enteral nutrition, were involved in the study up to the following two criterias: 1. when the energy provided by enteral nutrition up to 60% of the total energy requirement; 2. fasting venous blood-glucose >=160mg/dl (8.8mmol/L) the very day or Intravenous infusion of glucose versus regular insulin dosage(Glu:RI)<=10:1 the day before the very day.

Exclusion criteria

Exclusion criteria: 1. encyesis; 2. brain death state; 3. severe basic diseases not be cured; 4. terminal stage not recovery.

Design outcomes

Primary

MeasureTime frame
blood glucose;—

Countries

China

Contacts

Public ContactXu Yuan
xyuan76@163.com+86 13911800715

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026