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Prophylactic Dextrose Gel for Newborns at High-risk for Hypoglycemia

Primary Purpose

Hypoglycemia, Infant, Small for Gestational Age, Premature Birth of Newborn

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
40% Dextrose gel
Sponsored by
Baylor University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypoglycemia focused on measuring dextrose gel, newborn hypoglycemia, late preterm infant, large for gestational age, small for gestational age, prophylactic, neonatal hypoglycemia

Eligibility Criteria

undefined - 1 Hour (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Gestational age above 35 weeks
  • Infants less than 1 hour of age
  • Infants with informed parental consent
  • Infants who are born at the Harris Health Ben Taub Hospital in Houston, TX

Exclusion Criteria:

  • Infants with known metabolic, genetic, or congenital anomalies
  • Infants not expected to survive the neonatal period
  • Infants determined later to have a metabolic, genetic, or congenital anomaly that was not immediately obvious in the newborn period
  • Hypoglycemic infants with symptoms
  • Infants transferred to the Level 3 NICU for other reasons

Sites / Locations

  • Ben Taub Harris Health Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

CONTROL

Dextrose Gel

Arm Description

Infants at risk for transient neonatal hypoglycemia following standard-of-care.

Infants given 40% Dextrose gel (0.5ml/kg) in the buccal mucosa after their first feed, within the first hour of life.

Outcomes

Primary Outcome Measures

Prophylactic administration of dextrose gel
Give infants who meet criteria for high-risk and whose parents have consented one dose of prophylactic 40% dextrose gel (0.5ml/kg) after first feed. Assess glucose level after 1 feed and 1 application of dextrose gel, and admission to the NICU, compared to controls with similar risk factors who are not treated prophylactically.
Treatment failure of at-risk infants
Infants at-risk (IDM, late preterm, SGA, LGA, estimated fetal weight below 2.5kg or above 4kg, IUGR, or poor feeding) will be followed until hospital discharge to measure NICU admission data and glucose values during hospitalization.

Secondary Outcome Measures

Full Information

First Posted
August 12, 2015
Last Updated
November 16, 2016
Sponsor
Baylor University
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1. Study Identification

Unique Protocol Identification Number
NCT02523222
Brief Title
Prophylactic Dextrose Gel for Newborns at High-risk for Hypoglycemia
Official Title
Prophylactic Dextrose Gel for Newborns at High-risk for Hypoglycemia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
July 2016 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baylor University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This will be a quasi-experimental study comparing blood glucose values 30 minutes after feeding alone or feeding + 40% dextrose gel in newborns at risk for transient neonatal hypoglycemia.
Detailed Description
BACKGROUND: Low blood sugar in newborns affects about 10% of all deliveries and about 50% of newborns with identified risk factors and is associated with poor long-term neurodevelopmental outcomes. Risk factors for transient neonatal hypoglycemia include infants of diabetic mothers, infants who are large or small for gestational age, infants with intrauterine growth restriction, and late-preterm infants. GAP: Current standard of care recommends asymptomatic infants to receive intravenous dextrose after becoming hypoglycemic. International studies using dextrose gel have shown that the buccal mucosa is a promising alternative route, normalizes hypoglycemia, and decreases NICU admission. So far, no studies have published results about the efficacy of prophylactic dextrose gel. HYPOTHESIS: We hypothesize that the prophylactic treatment of newborns at-risk for transient neonatal hypoglycemia with 40% dextrose gel will raise blood sugar levels by 15% compared to untreated controls. We hypothesize that 40% dextrose gel will prevent up to 50% of NICU admissions in this at-risk population compared to matched controls. METHODS: This will be a quasi-experimental study. The study population will include babies born at Harris Health Ben Taub Hospital and have risk factors for transient neonatal hypoglycemia. After the baby completes its first feed, he or she will be given a dose of oral dextrose gel. A blood sugar level will be checked after 30 minutes, per standard of care. One hundred at-risk infants will be identified and have written parental consent prior to delivery and receiving the prophylactic treatment. Five hundred additional matched controls with similar risk factors will be analyzed for comparison and will not receive treatment. RESULTS: Pending IMPACT: If the study proves the hypotheses are correct, prophylactic dextrose gel could be implemented in newborn nurseries around the country to prevent transient hypoglycemia, decrease NICU admission (and its associated costs, painful procedures, and separation from family), improve feeding quality, and potentially optimize neurodevelopmental outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoglycemia, Infant, Small for Gestational Age, Premature Birth of Newborn, Fetal Macrosomia, Intrauterine Growth Restriction, Complication of Prematurity, Neonatal Hypoglycemia
Keywords
dextrose gel, newborn hypoglycemia, late preterm infant, large for gestational age, small for gestational age, prophylactic, neonatal hypoglycemia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CONTROL
Arm Type
No Intervention
Arm Description
Infants at risk for transient neonatal hypoglycemia following standard-of-care.
Arm Title
Dextrose Gel
Arm Type
Active Comparator
Arm Description
Infants given 40% Dextrose gel (0.5ml/kg) in the buccal mucosa after their first feed, within the first hour of life.
Intervention Type
Dietary Supplement
Intervention Name(s)
40% Dextrose gel
Intervention Description
40% dextrose gel will be rubbed into the hypoglycemic infant's buccal mucosa at a dose of 0.5ml/kg.
Primary Outcome Measure Information:
Title
Prophylactic administration of dextrose gel
Description
Give infants who meet criteria for high-risk and whose parents have consented one dose of prophylactic 40% dextrose gel (0.5ml/kg) after first feed. Assess glucose level after 1 feed and 1 application of dextrose gel, and admission to the NICU, compared to controls with similar risk factors who are not treated prophylactically.
Time Frame
2 hours
Title
Treatment failure of at-risk infants
Description
Infants at-risk (IDM, late preterm, SGA, LGA, estimated fetal weight below 2.5kg or above 4kg, IUGR, or poor feeding) will be followed until hospital discharge to measure NICU admission data and glucose values during hospitalization.
Time Frame
4 days

10. Eligibility

Sex
All
Maximum Age & Unit of Time
1 Hour
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Gestational age above 35 weeks Infants less than 1 hour of age Infants with informed parental consent Infants who are born at the Harris Health Ben Taub Hospital in Houston, TX Exclusion Criteria: Infants with known metabolic, genetic, or congenital anomalies Infants not expected to survive the neonatal period Infants determined later to have a metabolic, genetic, or congenital anomaly that was not immediately obvious in the newborn period Hypoglycemic infants with symptoms Infants transferred to the Level 3 NICU for other reasons
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey R Kaiser, MD, MS
Organizational Affiliation
Baylor College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ben Taub Harris Health Hospital
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
29605395
Citation
Coors SM, Cousin JJ, Hagan JL, Kaiser JR. Prophylactic Dextrose Gel Does Not Prevent Neonatal Hypoglycemia: A Quasi-Experimental Pilot Study. J Pediatr. 2018 Jul;198:156-161. doi: 10.1016/j.jpeds.2018.02.025. Epub 2018 Mar 28.
Results Reference
derived

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Prophylactic Dextrose Gel for Newborns at High-risk for Hypoglycemia

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