Effect of Administration of Combined Enteral Lactoferrin and Probiotic On Invasive Fungal Infections In Preterm Neonates
Primary Purpose
Fungal Infection
Status
Completed
Phase
Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
Lactoferrin Bovine
Lactoferrin Bovine and probiotics
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Fungal Infection focused on measuring Lactoferrin, Probiotic, Preterm
Eligibility Criteria
Inclusion Criteria:
- 80 preterm
- ≤ 36 weeks gestational age
- >/ = 72 hours of life
Exclusion Criteria:
- Nothing per os
- Congenital anomalies.
- Suspected inborn error of metabolism.
- Prophylaxis antifungal drugs
Sites / Locations
- Ain Shams University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Lactoferrin Bovine group
Lactoferrin Bovine with probiotics group
Placebo group
Arm Description
Group A (20 preterm neonates) which will receive lactoferrin (100mg/day)
Group B (20 preterm neonates) which will receive lactoferrin (100mg/day) in combination with the probiotic
Group C (40 preterm neonates) which is a placebo group.
Outcomes
Primary Outcome Measures
Number of participants with invasive fungal infection (IFI)
Efficacy of enteral lactoferrin either alone or in combination with the probiotic Lactobacillus Delbrueckii and Lactobacillus Fermentum in the prevention of invasive fungal infections in preterm infants through analyzing the incidence rates of invasive fungal infection (IFI) in all groups using Sabouraud agar for detecting Candida species and Hichrome agar to detect other fungal types.
Secondary Outcome Measures
Number of patients who received packed RBC in each group
The number of patients who received packed RBC in each group from time of enrollment till the 30th day of life
Days on inotropic support in each group
Define how many days required for inotropic support in each group
Days on mechanical ventilation in each group
Define how many days required for mechanical ventilation support in each group
Days of NICU admission in each group
Define how many days patients in each group were admitted in the NICU
Number of participants with Necrotizing enterocolitis in each group
Define the rate of NEC occurrence in each group
Mortality in each group
Define the number of mortality in each group
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05283278
Brief Title
Effect of Administration of Combined Enteral Lactoferrin and Probiotic On Invasive Fungal Infections In Preterm Neonates
Official Title
Effect of Administration of Combined Enteral Lactoferrin and Probiotic On Invasive Fungal Infections In Preterm Neonates
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
February 10, 2020 (Actual)
Primary Completion Date
March 27, 2021 (Actual)
Study Completion Date
April 27, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
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
The risk for invasive fungal infections is high in very low birth weight (VLBW) infants (< 1500 g) and highest for infants born at the youngest gestational ages who survive past the immediate postnatal period.
Invasive fungal infections (IFIs) represent an increasing cause of severe morbidity and mortality in most neonatal intensive care units.
Lactoferrin (LF) is secreted by epithelial cells into exocrine fluids: seminal fluid, tears, saliva, uterine secretions, and milk. LF is involved in innate immunity mechanisms with several documented anti-infective properties, including antifungal activity.
Probiotics are microorganisms that are believed to provide health benefits when consumed.
It is possible to adopt measures to modify the flora in our bodies and to replace the harmful microbes by useful microbes.
There are certain commercially available strains of probiotic bacteria from the Bifido bacterium and Lactobacillus genera when taken by mouth in daily doses possess treatment efficacy
Detailed Description
Bovine LF alone or in combination of probiotics (Lactobacillus Delbrueckii and Lactobacillus Fermentum) can be used in prevention of invasive fungal infection in preterm neonates admitted to the NICU. So, this randomized interventional study aimed at evaluation of the efficacy and safety of enterally administered bovine LF alone or in combination of probiotics (Lactobacillus Delbrueckii and Lactobacillus Fermentum) in comparison to placebo in preterm neonates, through studying blood culture for fungal infection at enrollment, day 7, 14, 21 and 28 using Sabouraud agar for detecting Candida species and Hichrome agar to detect other fungal types ( primary outcome), and to compare length of hospital stay (LOS), use and duration of drug intake as antibiotics and inotropes, use and duration of mechanical ventilation, rate of increase of enteral feeding, time to reach full enteral intake, signs of feeding intolerance, complete blood count (CBC), C reactive protein (CRP), packed red blood cell transfusion (PRBCs) and mortality between the 3 groups as (secondary outcome).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fungal Infection
Keywords
Lactoferrin, Probiotic, Preterm
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lactoferrin Bovine group
Arm Type
Active Comparator
Arm Description
Group A (20 preterm neonates) which will receive lactoferrin (100mg/day)
Arm Title
Lactoferrin Bovine with probiotics group
Arm Type
Active Comparator
Arm Description
Group B (20 preterm neonates) which will receive lactoferrin (100mg/day) in combination with the probiotic
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Group C (40 preterm neonates) which is a placebo group.
Intervention Type
Drug
Intervention Name(s)
Lactoferrin Bovine
Other Intervention Name(s)
Pravotin®
Intervention Description
Lactoferrin granules (Pravotin®) in a dose of 100 mg /kg/day starting from birth to the 30th day of life for neonates in group A
Intervention Type
Combination Product
Intervention Name(s)
Lactoferrin Bovine and probiotics
Other Intervention Name(s)
Pravotin® plus Lacteol fort
Intervention Description
Lactoferrin granules (Pravotin®) in a dose of 100 mg /kg/day in combination with the probiotic Lactobacillus Delbrueckii and Lactobacillus Fermentum (Lacteol fort®) given in a dose of 5 billions starting from birth to the 30th day of life for neonates in group B
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo will be given starting from birth to the 30th day of life for neonates in group C.
Primary Outcome Measure Information:
Title
Number of participants with invasive fungal infection (IFI)
Description
Efficacy of enteral lactoferrin either alone or in combination with the probiotic Lactobacillus Delbrueckii and Lactobacillus Fermentum in the prevention of invasive fungal infections in preterm infants through analyzing the incidence rates of invasive fungal infection (IFI) in all groups using Sabouraud agar for detecting Candida species and Hichrome agar to detect other fungal types.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of patients who received packed RBC in each group
Description
The number of patients who received packed RBC in each group from time of enrollment till the 30th day of life
Time Frame
30 days
Title
Days on inotropic support in each group
Description
Define how many days required for inotropic support in each group
Time Frame
12 months
Title
Days on mechanical ventilation in each group
Description
Define how many days required for mechanical ventilation support in each group
Time Frame
12 months
Title
Days of NICU admission in each group
Description
Define how many days patients in each group were admitted in the NICU
Time Frame
12 monthes
Title
Number of participants with Necrotizing enterocolitis in each group
Description
Define the rate of NEC occurrence in each group
Time Frame
12 months
Title
Mortality in each group
Description
Define the number of mortality in each group
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
80 preterm
≤ 36 weeks gestational age
>/ = 72 hours of life
Exclusion Criteria:
Nothing per os
Congenital anomalies.
Suspected inborn error of metabolism.
Prophylaxis antifungal drugs
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hebatallah A Shaaban, MD
Organizational Affiliation
Doctor
Official's Role
Study Director
Facility Information:
Facility Name
Ain Shams University
City
Cairo
ZIP/Postal Code
11381
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
No
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Effect of Administration of Combined Enteral Lactoferrin and Probiotic On Invasive Fungal Infections In Preterm Neonates
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