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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04109833
Other study ID # 368/2019BO1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 27, 2019
Est. completion date October 2021

Study information

Verified date September 2019
Source University Hospital Tuebingen
Contact Natascha Köstlin-Gille, Dr. med.
Phone 0049-7071-2984743
Email natascha.koestlin@med.uni-tuebingen.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Neonatal Sepsis is one of the most common causes of death in preterm infants. Therefore, up to 80% of very low birth weight infants receive antibiotic therapy in their first week of life. Antibiotic therapy is one of the most important influencing factors for the establishment of the intestinal microbiome, which in turn modulates neonatal immune development. In this pilot study, it will be investigated, if antibiotic therapy in the first week of life influences the vaccination response of preterm infants.


Description:

The aim of the study is to compare antibody titers against Hepatitis B, Polio, Pertussis, Haemophilus influenza B, Tetanus, Diphteria and Pneumococcus in very low birth weight infants (VLBWI) infants who received antibiotic therapy in their first week of life and who did not. In this pilot study, 20 VLBWI infants will be included (10 per group). Infants will be matched fo age and gender.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date October 2021
Est. primary completion date October 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 24 Weeks to 28 Weeks
Eligibility Inclusion Criteria:

- born at University Hospital Tübingen

- at least one dose of antibiotics within the first week of life

Exclusion Criteria:

- genetic disorders

- chronic infections

- hematological disorders

- immunoglobulins within the first 60 days of life

- immunological disorders

- infants from Hepatitis B positive mothers

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
ABT
any antibiotic therapy in the first week of life

Locations

Country Name City State
Germany University Hospital Tübingen Baden-Württemberg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary vaccination reaction measurement of antibody titers for Hepatitis B, Polio, Pertussis, Haemophilus Influenza B, Tetanus, Diphteria and Pneumococcus 4 months after the first vaccination (at an age of 6 months) 7 months
Secondary Microbiome composition microbiome analyses of stool samples at age 14 days and corrected 4 months 7 months
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