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The effect of calorie intake on Intensive Care Unite patients

comparative clinical outcome in Hypocaloric vs. Fullcaloric Enteral feeding during the first week of Hospitalization in Intensive Care Unite Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120525009856N6
Enrollment
70
Registered
2018-03-26
Start date
2018-03-30
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Patients of intensive care unit.

Interventions

Intervention 1: Intervention group: Patients in the intervention group will receive Hypocaloric diet. After hemodynamic stabilization, enteral nutrition support will be started during the first 24-48

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with expected length of hospitalization in Intensive Care Unite for at least 94 hours adult patients, 18 to 65 y old cannot eat sufficiently

Exclusion criteria

Exclusion criteria: body mass index (BMI) less than 18.5 mechanical ventilation

Design outcomes

Primary

MeasureTime frame
Aspartate amino transferase. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: Spectrophotometer.;Alanine amino transferase. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: Spectrophotometer.;Reactive Protein C. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: Autoanalyser.;High density lipoprotein. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: HDL kit.;Triglyceride. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: kit TG.;Cholesterol. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: Cholesterol Kit.;Low density lipoprotein. Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: Calculate with Friedewald formula.;Evaluation of electrolytes (sodium, potassium, magnesium, phosphorus). Timepoint: Before intervention, after intervention and one week after intervention. Method of measurement: Electrolyte analyzer.;Fasting blood sugar. Timepoint: Every day for two weeks. Method of measurement: Avtanalizer device.;Multinational defect. Timepoint: Time intervals 24, 48, 96 hours and the end of intervention. Method of measurement: Sofa questionnaire.

Secondary

MeasureTime frame
Insulin received. Timepoint: Every day for two weeks. Method of measurement: questionnaire.;Infection rate. Timepoint: Followed for 28 days. Method of measurement: questionnaire.;Duration of ventilator dependence. Timepoint: Followed for 28 days. Method of measurement: questionnaire.;Mortality. Timepoint: Followed for 28 days. Method of measurement: questionnaire.;Number of hospital admissions days in the intensive care unit. Timepoint: Followed for 28 days. Method of measurement: questionnaire.;Number of hospital admissions days. Timepoint: Followed for 28 days. Method of measurement: questionnaire.;Digestive complications. Timepoint: Every day for two weeks. Method of measurement: questionnaire.;Gastrointestinal intolerance. Timepoint: Every day for two weeks. Method of measurement: questionnaire.;Calorie intake. Timepoint: Every day for two weeks. Method of measurement: questionnaire.;Percentage of protein intake. Timepoint: Every day for two weeks. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyede Zeinab Mousavian

Kermanshah University of Medical Sciences

sz.mousavian@kums.ac.ir+91 83382 81991

Outcome results

None listed

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