Comparison of intensive versus conventional glycaemic control in patients on parentral nutritio
Not Applicable
- Conditions
- Hyperglycemia resulted from parenteral nutrition.Hyperglycaemia, unspecified
- Registration Number
- IRCT201111158108N1
- Lead Sponsor
- Mashhad medical sciences university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
patients aged 18 years or older with GCS 4-9 with muscle erosion, diarrhea or high residue that couldn’t feed through oral or enteral rout, were eligible for enrolling into the study. Patients on parentral nutrition criteria received at least 50% of their calorie from parenteral nutrition. Exclusion criteria: Patients with liver; kidney; heart; pancrease failure and or diabetes
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hyperglycemia. Timepoint: Every 2 hours in tight control group- every 12 hours in conventional group. Method of measurement: Glucometer Kit.
- Secondary Outcome Measures
Name Time Method During of hospital and ICU stay, mortality. Timepoint: 14 & 28 days after intervention. Method of measurement: Observe & phone number.