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Effect of Vitamin A in the Treatment of Neonatal Sepsis and Necrotizing Enterocolitis

Primary Purpose

Sepsis, Necrotizing Enterocolitis, Meningitis

Status
Completed
Phase
Phase 3
Locations
Bangladesh
Study Type
Interventional
Intervention
Vitamin A
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring vitamin A, Treatment, neonates, newborn, sepsis, necrotizing enterocolitis, meningitis, pneumonia

Eligibility Criteria

1 Day - 28 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • newborns less than 29 days with clinical sepsis

Exclusion Criteria:

  • healthy infants
  • major congenital abnormalities
  • known inborn error(s) of metabolism
  • chronic disorders of other organs (e.g. cholestasis)
  • definite or severe NEC (> stage 2)
  • congenital heart disease
  • Infants receiving VA supplements
  • Infants requiring mechanical ventilation
  • Infant is unconscious

Sites / Locations

  • Dhaka Shishu Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

1

2

3

4

Arm Description

Sepsis - vitamin A

Sepsis - placebo

NEC - vitamin A

NEC - Placebo

Outcomes

Primary Outcome Measures

Disease Mortality

Secondary Outcome Measures

Inflammatory cytokine concentration
Duration of inflammation
Disease progression in NEC patients

Full Information

First Posted
June 27, 2008
Last Updated
September 24, 2013
Sponsor
Johns Hopkins University
Collaborators
Bill and Melinda Gates Foundation, United States Agency for International Development (USAID), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00707785
Brief Title
Effect of Vitamin A in the Treatment of Neonatal Sepsis and Necrotizing Enterocolitis
Official Title
Effect of Vitamin A in the Treatment of Sepsis and Necrotizing Enterocolitis in Hospitalized Neonates
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Johns Hopkins University
Collaborators
Bill and Melinda Gates Foundation, United States Agency for International Development (USAID), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to determine whether vitamin A can improve survival and facilitate recovery from sepsis and necrotizing enterocolitis in hospitalized neonates.
Detailed Description
Sepsis and necrotizing enterocolitis (NEC) are leading causes of morbidity and mortality in neonates. Studies have shown that early reversal of the signs associated with severe disease is an important prognostic factor during acute illness. Vitamin A deficiency is widespread among children, including neonates, in developing countries. Vitamin A plays an important role in mediating immune responses and in maintaining epithelial integrity. For this reason vitamin A supplementation during the acute phase of neonatal infection could work synergistically with present antibiotic regimens in promoting early reversal of signs associated with adverse outcome and shorten the total duration of clinical illness. The purpose of the proposed hospital-based clinical trial is to evaluate the efficacy of vitamin A supplementation on reducing the morbidity and mortality among neonates hospitalized with sepsis (n=366) and NEC(n=150). Enrolled subjects will be randomized at the time of hospitalization to receive one dose of either 50,000 IU of vitamin A or placebo at enrollment, in addition to standard antibiotic therapy. We will compare the proportion of treatment failures in sepsis patients, the frequency of disease progression and mortality in NEC patients, and the time to clinical recovery and discharge between treatment groups. In addition, the study will determine whether vitamin A reduces pro-inflammatory cytokine levels; elevated host inflammatory cytokines are thought to contribute to the severity of both conditions. If vitamin A is found to be efficacious in the treatment of sepsis and NEC it could present a needed cost-effective approach to decreasing the global morbidity, mortality and the economic cost associated with neonatal sepsis and NEC in the developing world.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Necrotizing Enterocolitis, Meningitis, Pneumonia
Keywords
vitamin A, Treatment, neonates, newborn, sepsis, necrotizing enterocolitis, meningitis, pneumonia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
424 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Sepsis - vitamin A
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Sepsis - placebo
Arm Title
3
Arm Type
Experimental
Arm Description
NEC - vitamin A
Arm Title
4
Arm Type
Placebo Comparator
Arm Description
NEC - Placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin A
Other Intervention Name(s)
Retinol
Intervention Description
50,000 IU of Vitamin A 50,000 IU of vegetable oil
Primary Outcome Measure Information:
Title
Disease Mortality
Time Frame
prospective
Secondary Outcome Measure Information:
Title
Inflammatory cytokine concentration
Time Frame
prospective
Title
Duration of inflammation
Time Frame
prospective
Title
Disease progression in NEC patients
Time Frame
prospective
Other Pre-specified Outcome Measures:
Title
Treatment failure
Time Frame
prospective
Title
Time to recovery from severe illness
Time Frame
prospective

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
28 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: newborns less than 29 days with clinical sepsis Exclusion Criteria: healthy infants major congenital abnormalities known inborn error(s) of metabolism chronic disorders of other organs (e.g. cholestasis) definite or severe NEC (> stage 2) congenital heart disease Infants receiving VA supplements Infants requiring mechanical ventilation Infant is unconscious
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian L Coles, PhD
Organizational Affiliation
Johns Hopkins Bloomberg School of Public Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dhaka Shishu Hospital
City
Dhaka
Country
Bangladesh

12. IPD Sharing Statement

Learn more about this trial

Effect of Vitamin A in the Treatment of Neonatal Sepsis and Necrotizing Enterocolitis

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