Database for tracking neonatal infections
Neonatal Infection Surveillance Database
This study is creating a system to track and understand bacterial infections in newborns in the UK to help doctors respond quickly and improve care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 12000 (estimated) |
| Ages | 1 Minute to 12 Months |
| Sex | All |
| Sponsor | St George's, University of London Academic / other |
| Locations | 1 site (London) |
| Trial ID | NCT05742490 on ClinicalTrials.gov |
What this trial studies
The NeonIN surveillance database is designed to actively monitor bacterial infections in neonates across a network of neonatal units in the UK. It utilizes standardized definitions and microbiological techniques to ensure accurate data collection and analysis. By capturing real-time data on episodes of invasive neonatal infections, the database facilitates timely interventions and enhances understanding of infection patterns. Clinical, demographic, and microbiological information is gathered through a secure web-based platform, allowing for rapid analysis and reporting.
Who should consider this trial
Good fit: Ideal candidates for this study are infants in participating neonatal units who have experienced an episode of infection with a positive culture.
Not a fit: Patients who do not have a diagnosed episode of neonatal infection will not benefit from this study.
Why it matters
Potential benefit: If successful, this database could significantly improve the management and treatment of neonatal infections, leading to better outcomes for affected infants.
How similar studies have performed: Other studies utilizing similar surveillance approaches have shown success in improving infection management and outcomes in neonatal care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Infants on participating Neonatal Units who have an episode of infection with a positive culture Exclusion Criteria: \-
Where this trial is running
London
- St George's University of London — London, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Eva Galiza, MD — St George's, University of London
- Study coordinator: Sana Ibrahim, BSc
- Email: sibrahim@sgul.ac.uk
- Phone: +44 (0)208 725 5382
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.