Zinc Supplementation In Very Low Birth Weight Infants-A Randomised Controlled Trial
Primary Purpose
Preterm Infant, Effect of Drugs, Zinc Deficiency Disease
Status
Completed
Phase
Phase 4
Locations
Turkey
Study Type
Interventional
Intervention
Zinc Sulfate
Sponsored by
About this trial
This is an interventional prevention trial for Preterm Infant
Eligibility Criteria
Inclusion Criteria:
- < 32 weeks gestational age and/or <1500 gr birth weight
- Born in the study hospital
- Being able to be fed enterally, even in very small amounts, regardless of the volume of the nutrient
Exclusion Criteria:
- Major Congenital malformations and/or critical congenital heart defects
- Born in another hospital
- Severe birth asphyxia
- Babies on the intervention arm who did not continue Zinc supplementation during the study period
- No consent from the family
- Death before the 7th day of life
Sites / Locations
- Izmir Democracy University Faculty of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Zinc intervention
Control
Arm Description
9 mg/day Zinc suspension via og tube along with the routinely used standard multivitamin product containing 3 mg daily dose of Zn, started on day 7 until discharge from hospital
These infants received only standard commercial multivitamin product containing 3 mg daily dose of Zn
Outcomes
Primary Outcome Measures
Incidence of feeding intolerance
Secondary Outcome Measures
Duration of hospitalization
Number of participants with necrotising enterocolitis (stage≥2)
Incidence of mortality
Number of participants with late onset sepsis
Number of participants with retinopathy of prematurity
Number of participants with bronchopulmonary dysplasia
Full Information
NCT ID
NCT05311540
First Posted
May 19, 2019
Last Updated
February 3, 2023
Sponsor
Zekai Tahir Burak Women's Health Research and Education Hospital
Collaborators
Ankara City Hospital Bilkent
1. Study Identification
Unique Protocol Identification Number
NCT05311540
Brief Title
Zinc Supplementation In Very Low Birth Weight Infants-A Randomised Controlled Trial
Official Title
Zinc Supplementation In Very Low Birth Weight Infants-A Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
March 14, 2014 (Actual)
Primary Completion Date
March 2, 2015 (Actual)
Study Completion Date
April 20, 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zekai Tahir Burak Women's Health Research and Education Hospital
Collaborators
Ankara City Hospital Bilkent
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Zinc (Zn) is a structural component of human body and is a crucial element for a wide variety of cascades that take place in almost all organ systems.
Due to many reasons, preterm infants are generally believed to be naturally in a negative Zn balance during the early periods of life.
Regulation of intestinal Zn absorption of preterms is unrelated to infant's Zn status.
There still is a lack of knowledge in the possible relation of Zn deficiency and development of NEC and/or feeding intolerance in preterm infants.
Even if Zn is studied as an adjunct treatment for neonates and young infants with sepsis and found to reduce treatment failure in these high risk population, data in preventing infectious diseases in preterm infants is still lacking.
Detailed Description
Background and Objectives: Preterm infants have high zinc (Zn) requirements and are generally believed to be in a negative Zn balance in the early period of life. In this study, we aimed to investigate the effect of high dose Zn supplementation in very low birth weight (VLBW) infants on feeding intolerance and development of mortality and/or morbidities including necrotizing enterocolitis (NEC), late-onset sepsis (LOS).
Methods: This is a prospective randomized trial. VLBW preterm infants with gestational age of <32 weeks were randomly allocated on the seventh day of life to receive extra amount of supplemental zinc along with the enteral feedings or not, besides regular low dose supplementation, from enrollment until discharge. Outcome measures were feeding intolerance, NEC (stage≥2), LOS and mortality.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Infant, Effect of Drugs, Zinc Deficiency Disease
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Sequential Assignment
Masking
ParticipantInvestigator
Masking Description
An independent physician not involved in the study conducted the random assignment process. The investigators who were blinded to the randomisation process closely followed up the enrolled infants for any evidence of feeding intolerance and/or NEC, late-onset sepsis (LOS), bronchopulmonary dysplasia (BPD), hemodynamically significant patent ductus arteriosus (hsPDA), intraventricular hemorrhage (IVH), retinopathy of prematurity (ROP) along with other possible neonatal morbidities and signs of toxicity or side effects (adverse events)
Allocation
Randomized
Enrollment
195 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Zinc intervention
Arm Type
Experimental
Arm Description
9 mg/day Zinc suspension via og tube along with the routinely used standard multivitamin product containing 3 mg daily dose of Zn, started on day 7 until discharge from hospital
Arm Title
Control
Arm Type
No Intervention
Arm Description
These infants received only standard commercial multivitamin product containing 3 mg daily dose of Zn
Intervention Type
Drug
Intervention Name(s)
Zinc Sulfate
Primary Outcome Measure Information:
Title
Incidence of feeding intolerance
Time Frame
through study completion, an average of 6 months
Secondary Outcome Measure Information:
Title
Duration of hospitalization
Time Frame
through study completion, an average of 6 months
Title
Number of participants with necrotising enterocolitis (stage≥2)
Time Frame
through study completion, an average of 6 months
Title
Incidence of mortality
Time Frame
through study completion, an average of 6 months
Title
Number of participants with late onset sepsis
Time Frame
through study completion, an average of 6 months
Title
Number of participants with retinopathy of prematurity
Time Frame
through study completion, an average of 6 months
Title
Number of participants with bronchopulmonary dysplasia
Time Frame
through study completion, an average of 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Days
Maximum Age & Unit of Time
9 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
< 32 weeks gestational age and/or <1500 gr birth weight
Born in the study hospital
Being able to be fed enterally, even in very small amounts, regardless of the volume of the nutrient
Exclusion Criteria:
Major congenital malformations and/or critical congenital heart defects
Born in another hospital
Severe birth asphyxia
Severe sepsis
Previous early-onset NEC history
Infants on the intervention arm who did not continue Zinc supplementation during the study period
Hemodynamically unstability
Infants nil per os
No consent from the family
Death before the 7th day of life
Facility Information:
Facility Name
Izmir Democracy University Faculty of Medicine
City
Izmir
ZIP/Postal Code
35290
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
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Zinc Supplementation In Very Low Birth Weight Infants-A Randomised Controlled Trial
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