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Study identifier: NCT07490912 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Neonatal Data and Biobank to Study Factors Influencing Development in Preterm Infants Born at <32 Weeks' Gestation and/or <1500 g Birth Weight

Condition: Preterm Infant Development · Preterm Infant Health · Prematurity Complications  ·  Sponsor: University Hospital of Cologne

PhaseN/A
Planned participants1300
Who can joinAll sexes, N/A to 18 Years
Healthy volunteersNo

About this study

The Neo-Life project aims to establish a prospective neonatal data and biobank to investigate factors influencing the short- and long-term development of very preterm infants. Advances in neonatal care have significantly improved survival rates of infants born with a gestational age of less than 32 weeks and/or a birth weight below 1500 g. However, these infants remain at high risk for multiple complications affecting neurological, pulmonary, cardiovascular, renal, and other organ systems, which may lead to long-term morbidity and reduced quality of life. Identifying early risk and protective factors is therefore essential to improve outcomes and develop targeted interventions. The primary objective of the project is the prospective and structured collection of clinical data as well as biological samples within a standardized interdisciplinary follow-up program for preterm infants. The study aims to identify biological, clinical, and environmental factors associated with the development and long-term outcomes of different organ systems. The study population includes infants born with a gestational age of less than 32 weeks and/or a birth weight below 1500 g who receive care at the perinatal center of the University Hospital Cologne. Participation requires informed consent from the parents or legal guardians. There are no specific exclusion criteria. Participants will be followed within the established preterm follow-up program over several years, allowing longitudinal asses…

This description comes directly from the study's public registry record.

Talk to the study team

Charlotte S Schömig, Dr. med.  ·  +49 221 478 85663  ·  charlotte.schoemig@uk-koeln.de

Angela Kribs, Apl. Prof. Dr.  ·  +49 221 478 85663  ·  angela.kribs@uk-koeln.de

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital CologneCologne, North Rhine-Westphalia, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT07490912