Comparison of Cue based Feeding and Volume Based Feeding on Blood Glucose of preterm infants
Not Applicable
- Conditions
- Condition 1: Hypoglycemia. Condition 2: Prematurity.Hypoglycemia, unspecifiedPreterm newborn, unspecified weeks of gestationE16.2P07.30
- Registration Number
- IRCT20220704055362N2
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 122
Inclusion Criteria
Premature babies with a corrected age of 32 weeks and older
Full enteral feeding has been tolerated and parentral nutrition has been discontinued
Parental consent
Exclusion Criteria
Need for invasive and/or non invasive mechanical ventilation
Congenital abnormalities
Gastrointestinal surgery
Intra Ventricular Hemorrhage grade 3 or more
Swallowing disorder
Lack of parental consent
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood glucose. Timepoint: From the time of entry into the study for 3 days with intervals of every 6 hours. Method of measurement: Capillary blood glucose test from the heel with a glucometer.
- Secondary Outcome Measures
Name Time Method Episodes of feeding intolerance. Timepoint: From the time of entering the study for 3 days, after each feeding (every 3 to 4 hours). Method of measurement: Report of caregiver (nurse/mother) and importing in the checklist.;The rate of weight gain of neonates. Timepoint: From the time of entering the study till the day of discharge, daily assessment. Method of measurement: Weighing with a digital scale by the caregiver every morning.;The number of days the baby is hospitalized. Timepoint: From the time of entering the study till the day of discharge, one time at discharge day. Method of measurement: Calculation of the number of days of hospitalization of the baby from the time of entering the study to the day of discharge. Baby's medical record.