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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02035943
Other study ID # 127
Secondary ID
Status Completed
Phase N/A
First received December 1, 2011
Last updated January 13, 2014
Start date January 2008
Est. completion date December 2008

Study information

Verified date January 2014
Source Policlinico Hospital
Contact n/a
Is FDA regulated No
Health authority Italy: Ministry of Health
Study type Interventional

Clinical Trial Summary

In this study the investigators want to comare safety and efficacy of two different metods to administrate insulin during parenteral nutrition.


Description:

In this study the investigators want to compare safety and efficacy of two different metods to administrate insulin during parenteral nutrition.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- Critical ill patients undergone parenteral nutrition

Exclusion Criteria:

- Acute cerebral injury, pregnancy

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms

  • Critical Ill Patient Undergone Parenteral Nutrition

Intervention

Dietary Supplement:
Insulin separated
separate continuos infusion of insulin
Insulin added to parenteral nutrition
Insulin added to parenteral nutrition

Locations

Country Name City State
Italy Policlinico Hospital Milano MI

Sponsors (1)

Lead Sponsor Collaborator
Policlinico Hospital

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of glucose level control out of range (80-110 mg/dl) ICU stay (a week on average) Yes