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Comparison of intensive versus conventional glycaemic control in patients on parentral nutrition

Comparison of intensive versus conventional glycaemic control in patients on parentral nutrition in intensive care unit.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201111158108N1
Enrollment
32
Registered
2011-12-08
Start date
2011-02-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Hyperglycemia resulted from parenteral nutrition. Hyperglycaemia, unspecified

Interventions

Intervention 1: Intensive control: 50 unit regular insulin in 50 cc saline, continious insulin infusion, blood glucose control every 2 hours and insulin infusion according to chart, administration of
Treatment - Drugs
Intensive control: 50 unit regular insulin in 50 cc saline, continious insulin infusion, blood glucose control every 2 hours and insulin infusion according to chart, administration of this method in 1
Conventional control: blood glucose checking every 12 hours, regular insulin injection according to chart, administration of this method in 14 days.

Sponsors

Mashhad medical sciences university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hyperglycemia. Timepoint: Every 2 hours in tight control group- every 12 hours in conventional group. Method of measurement: Glucometer Kit.

Secondary

MeasureTime frame
During of hospital and ICU stay, mortality. Timepoint: 14 & 28 days after intervention. Method of measurement: Observe & phone number.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyede Neda Mousavi

Mashhad medical sciences university

mousavin881@mums.ac.irneda.mousavi@yahoo.com+98 51 1800 2382

Outcome results

None listed

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