Early Antibiotic Therapy and Vaccinations in Preterm Infants

Sponsor
University Hospital Tuebingen (Other)
Overall Status
Recruiting
CT.gov ID
NCT05563753
Collaborator
(none)
82
1
24
3.4

Study Details

Study Description

Brief Summary

Since the neonatal sepsis is still one of the most common causes of death in preterm infants up to 80% receive an perinatal antibiotic treatment. It is also known that an antibiotic treatment is one of the most important influences for the establishment of the intestinal microbiome. This again is important for the development of an healthy neonatal immunosystem. A pilot study showed that an antibiotic therapy in the first week of life had a negative influence on the vaccine titers of preterm infants.

In this study it will be further investigated if an early antibiotic treatment influences the development of the adaptive immunosystem in preterm infants and if this antibiotic treatment effects the development of the intestinal microbiome.

Condition or Disease Intervention/Treatment Phase

Detailed Description

The study wants to investigate the impact of the antibiotic treatment in the first week of live on the adaptive immunosystem. For this the antibody titers against Hepatitis B, Poliomyelitis, Pertussis, Haemophilus influenzae B, Tetanus, Diphtheria and Pneumococcus of very low birth weight infants (VLBWI) who receive an early antibiotic therapy will be compared with the antibody titers of infants who did not receive antibiotic treatment. Further the development of b- and t-cells will be tested.

To show the modulation of the intestinal microbiome through antibiotics stool samples of VLBWI with and without antibiotic therapy in first week of life will be tested for their composition and diversity as well as for the production of short-chained fatty acids (SCFA) In this study 82 VLBWI (42 per group) will be included. Infants will be matched by age and gender.

Study Design

Study Type:
Observational
Anticipated Enrollment :
82 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Impact of Early Antibiotic Therapy on Vaccination Response in Preterm Infants
Actual Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Sep 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
ABT in the first week of life

VLBWI with gestational age between 24+0 and 31+6 weeks of gestation with antibiotic treatment in the first week of life

Drug: ABT
any antibiotic therapy in the first week of life
Other Names:
  • any antibiotic therapy
  • no antibiotic therapy (ABT) in the first week of life

    VLBWI with gestational age between 24+0 and 31+6 weeks of gestation without antibiotic treatment in the first week of life

    Outcome Measures

    Primary Outcome Measures

    1. Vaccination response [7 Month]

      Measurement of antibody titers against Hepatitis B, Poliomyelitis, Pertussis, Haemophilus Influenzae B, Tetanus, Diphteria and Pneumococcus four month after the first received vaccination

    2. Analyses of b- and t-cells development [7 Month]

      Analyses of b- and t-cell development with the adjusted age of 4 moth

    Secondary Outcome Measures

    1. Microbiome analyses [7 Month]

      Analyses of the microbiome composition at the age of 14 days and adjusted age of 4 month

    2. Analyses of SCFA production of the intestinal microbiome [7 month]

      Analyses of SCFA production of the intestinal microbiome with the age of corrected 4 month

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    24 Weeks to 32 Weeks
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • born at University Hospital Tübingen

    • received at least one dose of antibiotics during the first week of life

    Exclusion Criteria:
    • genetic disorders

    • chronic infections

    • hematological disorders

    • treatment with immunoglobulins during the first 60 days of life

    • immunological disorders

    • infants with Hepatitis B positive mothers

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospial Tübingen Tübingen Baden-Württemberg Germany 72076

    Sponsors and Collaborators

    • University Hospital Tuebingen

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital Tuebingen
    ClinicalTrials.gov Identifier:
    NCT05563753
    Other Study ID Numbers:
    • 024/2022BO1
    First Posted:
    Oct 3, 2022
    Last Update Posted:
    Oct 12, 2022
    Last Verified:
    Sep 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 12, 2022