search
Back to results

A Pilot Randomized Controlled Trial for Antibiotic Exposure in Neonatal Sepsis Using Neutrophil CD64

Primary Purpose

Neonatal Early-onset Sepsis, Neonatal Late-onset Sepsis

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intervention is to stop antibiotics at 24h .
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neonatal Early-onset Sepsis focused on measuring Infant, Infection, Newborn, Antibiotics, Neutrophil CD64, Blood Culture

Eligibility Criteria

1 Hour - 5 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants undergoing a sepsis evaluation in the NICU

Exclusion Criteria:

  • They have a major life-threatening congenital malformation
  • The attending neonatologist has objections to the infant participating in the study

Sites / Locations

  • Yale-New Haven Children's Hospital NICU

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control (continue antibiotics) group

Study (discontinue antibiotics) group

Arm Description

The antibiotics will be continued for at least another 24h i.e. for 48h, pending blood culture results at 48h, as per standard practice in the NICU.

The intervention is to discontinue antibiotics at 24h, and he/she will be kept under observation in the NICU for at least an additional 24h, pending blood culture results at 48h.

Outcomes

Primary Outcome Measures

Number of infants with early-onset sepsis (EOS) and late-onset sepsis (LOS) randomized to either stopping or continuing antibiotics at 24h, based on the neutrophil CD64 measurement

Secondary Outcome Measures

Change in the Neutrophil CD64 Index value in neonates with/without exposure to antibiotics from 24h to 48h.

Full Information

First Posted
April 2, 2013
Last Updated
March 27, 2020
Sponsor
Yale University
search

1. Study Identification

Unique Protocol Identification Number
NCT01825421
Brief Title
A Pilot Randomized Controlled Trial for Antibiotic Exposure in Neonatal Sepsis Using Neutrophil CD64
Official Title
A Pilot Randomized Controlled Trial for Antibiotic Exposure in Neonatal Sepsis Using Neutrophil CD64
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Withdrawn
Why Stopped
No funding obtained
Study Start Date
October 2014 (undefined)
Primary Completion Date
January 2016 (Anticipated)
Study Completion Date
June 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Unnecessary and prolonged antibiotic therapy in newborn babies can have serious consequences including development of necrotizing enterocolitis (a serious, potentially life-threatening gastrointestinal illness in premature babies), late-onset infections, resistance to antibiotics, increased length of hospital stay, and death. Starting and continuing antibiotic therapy for blood culture-negative infections in the neonatal intensive care unit (NICU) is fairly common with numbers of such patients varying from 20%-90% of infants undergoing a sepsis evaluation in the NICU. While blood culture results are the gold standard, there is usually a delay of up to 48-72h before the results are known. Hence, initiation and continuation of antibiotic treatment are usually based on clinical evaluation and blood count criteria which do not possess high specificity or sensitivity, and may be unreliable in the first few hours after birth or in the early stages of infection. Since the investigators found that neutrophil CD64 (a type of protein found on the surface of a type of white blood cell that can be detected quickly in a very small amount of blood sample) has high accuracy for early detection of blood culture-proven infections in newborn babies, with extremely high negative predictive value (can identify babies definitively with no infection), the investigators will use this test to decide whether to stop or continue antibiotics in the NICU. The investigators hypothesis is that neutrophil CD64 values can be safely used to discontinue antibiotics in newborns suspected of having infections. The investigators aims are to utilize sequential measurements of CD64 values to stop antibiotics early in neonates being investigated for both early and late-onset infections in the NICU. This is a prospective, randomized, controlled (RCT) trial. The study population will be derived from the sub-set of all newborn infants who have undergone investigations for presence of infection in the NICU.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Early-onset Sepsis, Neonatal Late-onset Sepsis
Keywords
Infant, Infection, Newborn, Antibiotics, Neutrophil CD64, Blood Culture

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control (continue antibiotics) group
Arm Type
No Intervention
Arm Description
The antibiotics will be continued for at least another 24h i.e. for 48h, pending blood culture results at 48h, as per standard practice in the NICU.
Arm Title
Study (discontinue antibiotics) group
Arm Type
Active Comparator
Arm Description
The intervention is to discontinue antibiotics at 24h, and he/she will be kept under observation in the NICU for at least an additional 24h, pending blood culture results at 48h.
Intervention Type
Other
Intervention Name(s)
Intervention is to stop antibiotics at 24h .
Intervention Description
Stoppage of antibiotics at 24h in the intervention arm, randomization based on neutrophil CD64 values.
Primary Outcome Measure Information:
Title
Number of infants with early-onset sepsis (EOS) and late-onset sepsis (LOS) randomized to either stopping or continuing antibiotics at 24h, based on the neutrophil CD64 measurement
Time Frame
At 48h after initiation of antibiotics.
Secondary Outcome Measure Information:
Title
Change in the Neutrophil CD64 Index value in neonates with/without exposure to antibiotics from 24h to 48h.
Time Frame
At 48h after initiation of antibiotics.
Other Pre-specified Outcome Measures:
Title
Number of positive blood cultures in neonates from 24h to 48h with/without exposure to antibiotics.
Time Frame
At 48h after initiation of antibiotics.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Hour
Maximum Age & Unit of Time
5 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants undergoing a sepsis evaluation in the NICU Exclusion Criteria: They have a major life-threatening congenital malformation The attending neonatologist has objections to the infant participating in the study
Facility Information:
Facility Name
Yale-New Haven Children's Hospital NICU
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06520
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Pilot Randomized Controlled Trial for Antibiotic Exposure in Neonatal Sepsis Using Neutrophil CD64

We'll reach out to this number within 24 hrs