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Antibiotics and Gut Microbiota Among Newborn Infants

Primary Purpose

Surgical Wound Infection, Infection; Cesarean Section, Complications; Cesarean Section

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Cefuroxime
Sponsored by
Odense University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Surgical Wound Infection focused on measuring Randomized Controlled Trial, Caesarean Section, Surgical Site Infections, Wound Infections, Infectious Morbidity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 year
  • Women, who can read and understand Danish
  • A gestational age ≥ completed 28 weeks of gestation
  • Rupture of membranes and active labour (uterine contractions) is allowed.
  • BMI < 30

Exclusion Criteria:

  • Hypersensitivity to cefuroxime or to any other cephalosporin antibiotics
  • Previous immediate and/or severe hypersensitivity reaction to penicillin or any other beta-lactam antibiotic.
  • Systemic exposure to any antibiotic agent within 1 week before delivery Antibiotic indicated due to PROM, fever, group B Streptococcus or other indications at the time of caesarean section.
  • Women being immunologically incompetent (e.g. HIV positive)
  • Very sick newborn infants transferred to a neonatal intensive care unit and treated with antibiotics will be excluded from the study

Sites / Locations

  • Odense University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

preoperative antibiotic

postoperative antibiotic

Arm Description

iv Cefuroxime 1,5g administered 15-60 minutes before incision

iv Cefuroxime 1,5g administered after umbilical cord clamping

Outcomes

Primary Outcome Measures

Maternal: incidence of post-CS infection (endometritis, urinary tract infections and wound infection) in each study group
Infant: fecal microbiota at the tenth day of life

Secondary Outcome Measures

Maternal: Length of hospitalization
Maternal: readmissions to hospital on suspicion of postpartum infection following cesarean section
Antibiotic treatment
Infant: concentration of cefuroxime in blood samples
Infant: immunological analyses in blood samples on day 3

Full Information

First Posted
February 25, 2014
Last Updated
August 10, 2014
Sponsor
Odense University Hospital
Collaborators
University of Copenhagen, Aase and Ejnar Danielsens Foundation, Region of Southern Denmark, University of Southern Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT02072798
Brief Title
Antibiotics and Gut Microbiota Among Newborn Infants
Official Title
Antibiotic Prophylaxis for Postpartum Infections Following Caesarean Section
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Odense University Hospital
Collaborators
University of Copenhagen, Aase and Ejnar Danielsens Foundation, Region of Southern Denmark, University of Southern Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background Women undergoing Caesarean Section (CS) have an increased risk of postpartum infections compared to women undergoing vaginal delivery. In Denmark the incidence of post-CS infections is 7-10%. The most common infections are endometritis, Urinary tract infections (UTI) and wound infections (WI). Prophylactic antibiotics are effective in preventing postoperative infections and national guidelines recommend that antibiotics should be administered as a single dose immediately before surgical incision. CS is an exception to this pre-incision administration approach. National guidelines recommend administration of antibiotics after umbilical cord clamping to avoid exposure of the child to antibiotics before birth. Recent studies of antibiotic prophylaxis for CS suggest that prophylactic antibiotics administered before incision compared to after umbilical cord clamping may reduce post-CS infections by up to 50%. Two Cochrane reviews from 2012 criticize these types of studies for lack of data for outcomes on the baby and on late infection in the mother. At birth, all mammals must rapidly adapt to intake of complex milk nutrients via the gut and simultaneously tolerate the invasion of billions of microbes. This requires rapid maturation of the digestive and immune functions to avoid gut disorders and infections. Full-term, breast-fed infants normally adapt well, but factors such as caesarean birth, high hygiene levels, antibiotics treatment and formula feeding may inhibit immune development both short and long term. Birth by caesarean section in high-hygiene hospital environments, and widespread use of antibiotics, are factors that reduce gut microbiota density and diversity in the newborn for some time after birth. On the other hand, high-hygiene environments and antibiotics are essential tools to combat infections, especially for the weakest newborn infants. This pilot study will be a feasibility study to the original study, which examines the effect of change in timing of prophylactic antibiotics on the rate of post-CS infections (endometritis, UTI and WI). The pilot study focus on antibiotic and changes in the gut microbiota of newborn infants. The feasibility study will only include pregnant women in Odense with a body mass index below 30, and planned cesarean section.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Wound Infection, Infection; Cesarean Section, Complications; Cesarean Section
Keywords
Randomized Controlled Trial, Caesarean Section, Surgical Site Infections, Wound Infections, Infectious Morbidity

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
preoperative antibiotic
Arm Type
Active Comparator
Arm Description
iv Cefuroxime 1,5g administered 15-60 minutes before incision
Arm Title
postoperative antibiotic
Arm Type
Active Comparator
Arm Description
iv Cefuroxime 1,5g administered after umbilical cord clamping
Intervention Type
Drug
Intervention Name(s)
Cefuroxime
Other Intervention Name(s)
Cefuroxime "Fresenius Kabi"
Intervention Description
iv Cefuroxime 1,5g administered 15-60 minutes before incision versus iv Cefuroxime 1,5g administered after umbilical cord clamping
Primary Outcome Measure Information:
Title
Maternal: incidence of post-CS infection (endometritis, urinary tract infections and wound infection) in each study group
Time Frame
Within the first 30 days after surgery
Title
Infant: fecal microbiota at the tenth day of life
Time Frame
on the tenth day of life
Secondary Outcome Measure Information:
Title
Maternal: Length of hospitalization
Time Frame
Within the first 30 days after Caesarean Section
Title
Maternal: readmissions to hospital on suspicion of postpartum infection following cesarean section
Time Frame
Within the first 30 days after Caesarean Section
Title
Antibiotic treatment
Time Frame
within the first 30 days after Caesarean Section
Title
Infant: concentration of cefuroxime in blood samples
Time Frame
during the first 24 hours of life
Title
Infant: immunological analyses in blood samples on day 3
Time Frame
On the third day of life

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 year Women, who can read and understand Danish A gestational age ≥ completed 28 weeks of gestation Rupture of membranes and active labour (uterine contractions) is allowed. BMI < 30 Exclusion Criteria: Hypersensitivity to cefuroxime or to any other cephalosporin antibiotics Previous immediate and/or severe hypersensitivity reaction to penicillin or any other beta-lactam antibiotic. Systemic exposure to any antibiotic agent within 1 week before delivery Antibiotic indicated due to PROM, fever, group B Streptococcus or other indications at the time of caesarean section. Women being immunologically incompetent (e.g. HIV positive) Very sick newborn infants transferred to a neonatal intensive care unit and treated with antibiotics will be excluded from the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nana Hyldig, PhD student
Organizational Affiliation
Odense University Hospital, department of Plastic Surgery, University of Southern Denmark, Faculty of Health Sciences, institute of Clinical Research, research unit, department of Gynaecology and Obstetrics
Official's Role
Study Chair
Facility Information:
Facility Name
Odense University Hospital
City
Odense
State/Province
Fyn
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
31053348
Citation
Kamal SS, Hyldig N, Krych L, Greisen G, Krogfelt KA, Zachariassen G, Nielsen DS. Impact of Early Exposure to Cefuroxime on the Composition of the Gut Microbiota in Infants Following Cesarean Delivery. J Pediatr. 2019 Jul;210:99-105.e2. doi: 10.1016/j.jpeds.2019.03.001. Epub 2019 Apr 30.
Results Reference
derived
Links:
URL
http://www.neomune.ku.dk
Description
"The NEOMUNE centre" is a research platform aiming to improve clinical care of newborn infants, particular those born with developmental problems

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Antibiotics and Gut Microbiota Among Newborn Infants

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