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Clinical Trials/NCT04479254
NCT04479254CompletedNot Applicable

The Impact of Indirect Calorimetry Guided Medical Feeding Protocol on Clinical Outcomes in Critically Ill Patients

International Islamic University Malaysia2 sites in 1 country60 target enrollmentStarted: September 25, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
2
Primary Endpoint
ICU mortality

Study Overview

Brief Summary

Adequate nutritional support is an essential element for achieving favourable outcomes in critically ill patients. Therefore, an accurate determination of patients' energy needs is required to optimize nutritional support and reduce the harmful effects of under- and over-feeding. Currently, indirect calorimetry is considered as a gold standard for measuring energy expenditure during critical illness.

This randomized study aims to investigate the impact of indirect calorimetry guided nutrition therapy on clinical outcomes such as ICU. Mortality, hospital mortality, duration of mechanical ventilation, length of I.C.U./hospital stay and mascle wasting. The investigators hypothesis that nutrition therapy guided by IC will improve clinical outcomes in severely ill patients

Detailed Description

This is a single-blind randomized control study. Eligible participants are randomly assigned within 24 hrs of ICU. admission in two groups

  • Intervention group: The calorie needs will be determined by indirect calorimetry.
  • Control group: a routine standard weight-based equation (20-25kcal/kg ideal body weight/day) will be used to estimate the energy requirements of critically ill patients.

Daily energy and protein data will be recorded for a maximum of 12 evaluable days (nutritional days) or until death or discharge from ICU.while outcome data will be collected for a maximum of 28 days.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adult patients aged over 18 years old
  • Critically ill patients with me ical ventilation
  • Expected to have an ICU. stay of more than (3) days

Exclusion Criteria

  • Requirement for inspired oxygen content (FiO2) greater than 0.6
  • Patients on high-frequency ventilation
  • Patients with chest tubes that leak air/ Bronchopleural fistula
  • Patients with incompetent tracheal cuff
  • Patients inhaled nitric oxide therapy
  • Patients receiving continuous renal replacement therapy (CRRT) during IC measurement
  • Patients with pregnancy
  • Patients with burn injury
  • Patients infected with human immunodeficiency virus (HIV)
  • Patients with severe liver disease (Child-Pugh score C)
  • seizure activity
  • patients suffering from significant head trauma (GCS <8)
  • Patients with paraplegia and quadriplegia

Outcomes

Primary Outcomes

ICU mortality

Time Frame: 28 Days

Rate of mortality from all causes before or at day 28 in the ICU during the same ICU admission

Secondary Outcomes

  • Length of mechanical ventilation(28Days)
  • Length hospital stay(28 Days)
  • Hospital mortality(28Days)
  • Length of ICU stay(28 Days)
  • Muscle wasting(First 10 days of ICU admission)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohd Basri Mat Nor

Associate.Professor

International Islamic University Malaysia

Study Sites (2)

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