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Clinical Trials/CTRI/2024/03/064726
CTRI/2024/03/064726Not yet recruitingNot Applicable

Prevention of neonatal hypoglycemias with oral dextrose gel among high-risk neonates admitted in Tertiary care centre

Dr. Uthayashree P1 site in 1 country30 target enrollmentStarted: April 1, 2024Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
prevention of hypoglycemia among high risk neonates

Study Overview

Brief Summary

Glucose is the principal substrate for cerebral metabolism, and neonatal hypoglycemia causes damage in neuroglial cells and leads to adverse neurodevelopmental outcome.Approximately 25% of neonates are at risk for neonatal hypoglycemia. Some of these infants fail to normalize blood glucose levels by feed alone and require intravenous dextrose therapy. Preterm infants, small for gestational age (SGA), large for gestational age (LGA), infants of diabetic mothers are at high risk of requiring intravenous dextrose therapy due to persistent hypoglycemia.

 In this study, we aim to study about the use of oral dextrose gel (40%) in preventing hypoglycemia in at risk neonates which helps in better neurodevelopmental outcome and the use of oral dextrose gel in preventing hospital admission and early initiation of breastfeeding

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
0.00 Day(s) to 7.00 Day(s) (—)
Sex
All

Inclusion Criteria

  • •preterm, small for gestational age, large for gestational age, infants of diabetic mothers.

Exclusion Criteria

  • •sepsis, endocrine causes.

Outcomes

Primary Outcomes

prevention of hypoglycemia among high risk neonates

Time Frame: every 6th hourly for 72 hours of life

Secondary Outcomes

  • EARLY DISCHARGE RATE(1 week)

Investigators

Sponsor
Dr. Uthayashree P
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

DrUthayashree P

Gulbarga institute of medical sciences

Study Sites (1)

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