Effect of Oral Probiotic Supplementation on The Rate of Hospital Acquired Infection and Necrotizing Enterocolitis in Preterm Very Low Birth Weight Infants
Primary Purpose
Nosocomial Infection, Necrotizing Enterocolitis
Status
Completed
Phase
Phase 3
Locations
Thailand
Study Type
Interventional
Intervention
probiotics
Sponsored by
About this trial
This is an interventional treatment trial for Nosocomial Infection focused on measuring nosocomial infections, necrotizing enterocolitis, preterm infants, ver low birth weight, probiotics
Eligibility Criteria
Inclusion Criteria:
- Very Low Birth Weight (VLBW) preterm infants (Gestational age < 35 weeks , BW < 1500 g ) admitted to the NICU who survived the first 3 days of life
Exclusion Criteria:
- Infants with chromosome abnormality or severe congenital defects, especially gastrointestinal anomalies (e.g. omphalocele, gastroschisis, intestinal obstruction) and infants with unstable hemodynamic status
Sites / Locations
- Faculty of Medicine Chilalongkorn University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
study
control
Arm Description
Probiotics supplementation .
The control group received daily placebo liquid .
Outcomes
Primary Outcome Measures
incidence of nosocomial infections
Nosocomial infections , defined as any major infection occurring during the hospitalization, not earlier than 5 days of life.(sepsis, pneumonia, NEC, meningitis, omphalitis, osteomyelitis, soft tissue infection etc.). Sepsis was defined as a clinical syndrome of systemic illness accompanied by positive blood culture.
Secondary Outcome Measures
incidence of necrotizing enterocolitis (NEC)
necrotizing enterocolitis (NEC), which was identified and categorized by modified Bell's classification
feeding tolerance
the volume of feeding on day 7,14,21, and 28 of study
time to full enteral feeding
time required to reach full feeding at 150 ml/kg/day
Full Information
NCT ID
NCT01340469
First Posted
April 19, 2011
Last Updated
April 20, 2011
Sponsor
King Chulalongkorn Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01340469
Brief Title
Effect of Oral Probiotic Supplementation on The Rate of Hospital Acquired Infection and Necrotizing Enterocolitis in Preterm Very Low Birth Weight Infants
Official Title
Nosocomial Infections and Necrotizing Enterocolitis in Preterm Neonates Treated With Lactobacillus Acidophilus and Bifidobacterium Infantis in An Intensive Care Unit : A Randomized Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2011
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
June 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
King Chulalongkorn Memorial Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine whether oral probiotic supplementation could reduce the incidence of nosocomial infections in preterm infants.
Detailed Description
There are growing numbers of evidence indicating the beneficial effects of normal enteric flora (probiotics) with regard to the host defense against infection. In vitro and in vivo studies have shown that probiotics such as lactobacilli and bifidobacteria have inhibitory effects on other pathogenic bacteria.This evidence, along with the results of recent clinical studies, has demonstrated the beneficial effects of probiotics in the prevention of NEC in VLBW infants.However, most of the studies reported nosocomial infection as a secondary outcome and the findings were controversial regarding probiotics efficacy in preventing nosocomial infections. There is only one study that was aimed to investigate effects of probiotic on the incidence of nosocomial infection.
Given the potential benefit of probiotics against infection and the lack of clinical studies in this regard, we conducted a randomized clinical trial to determine whether probiotic supplementation (in the form of Lactobacillus acidophilus and Bifidobacterium infantis) could reduce nosocomial infection rate among preterm VLBW infants in a intensive care nursery setting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nosocomial Infection, Necrotizing Enterocolitis
Keywords
nosocomial infections, necrotizing enterocolitis, preterm infants, ver low birth weight, probiotics
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
160 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
study
Arm Type
Active Comparator
Arm Description
Probiotics supplementation .
Arm Title
control
Arm Type
Placebo Comparator
Arm Description
The control group received daily placebo liquid .
Intervention Type
Biological
Intervention Name(s)
probiotics
Other Intervention Name(s)
Infloran (Swiss Berna)
Intervention Description
Daily enteral probiotic supplementation (live Lactobacillus acidophilus and Bifidobacterium infantis) at a dose of 2.5 x 108 CFU of each strain once a day.The supplementation was started on the first day of enteral feeding and continued for at least 28 days or until discharge. The study drug was in liquid form and mixed with breast milk or formula before given to the infants. The preparation was made on a daily basis by one person who was not involved in the care of the infants.
Primary Outcome Measure Information:
Title
incidence of nosocomial infections
Description
Nosocomial infections , defined as any major infection occurring during the hospitalization, not earlier than 5 days of life.(sepsis, pneumonia, NEC, meningitis, omphalitis, osteomyelitis, soft tissue infection etc.). Sepsis was defined as a clinical syndrome of systemic illness accompanied by positive blood culture.
Time Frame
28 days or until discharge
Secondary Outcome Measure Information:
Title
incidence of necrotizing enterocolitis (NEC)
Description
necrotizing enterocolitis (NEC), which was identified and categorized by modified Bell's classification
Time Frame
28 days or until discharge
Title
feeding tolerance
Description
the volume of feeding on day 7,14,21, and 28 of study
Time Frame
28 days
Title
time to full enteral feeding
Description
time required to reach full feeding at 150 ml/kg/day
Time Frame
28 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Days
Maximum Age & Unit of Time
28 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Very Low Birth Weight (VLBW) preterm infants (Gestational age < 35 weeks , BW < 1500 g ) admitted to the NICU who survived the first 3 days of life
Exclusion Criteria:
Infants with chromosome abnormality or severe congenital defects, especially gastrointestinal anomalies (e.g. omphalocele, gastroschisis, intestinal obstruction) and infants with unstable hemodynamic status
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Santi Punnahitananda, M.D.
Organizational Affiliation
Chulalongkorn University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Medicine Chilalongkorn University
City
Bangkok
ZIP/Postal Code
10330
Country
Thailand
12. IPD Sharing Statement
Learn more about this trial
Effect of Oral Probiotic Supplementation on The Rate of Hospital Acquired Infection and Necrotizing Enterocolitis in Preterm Very Low Birth Weight Infants
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