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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
Zekai Tahir Burak Women's Health Research and Education Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preterm Infant

Eligibility Criteria

7 Days - 9 Days (Child)All SexesDoes not accept healthy volunteers

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

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
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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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