Clinical trial Recruiting at 1 site Observational

Investigating genetic factors in diseases affecting premature infants

Official title: Genetic Variants and Susceptibility to Diseases of Prematurity in Very Low Birth-Weight Infants

Run by Medical College of Wisconsin · NCT00710112 · Data updated 2026-11-12

This study is trying to see if certain genes and biomarkers can help us understand why some premature babies are more likely to develop serious health issues like lung disease and infections.

More Interstitial Lung Disease trials

Quick facts

Study typeObservational
SexAll
Enrollment1100 (estimated)
SponsorMedical College of Wisconsin
Academic / other
Locations1 site (Milwaukee, Wisconsin)
StatusRecruiting
StartedJune 2006
Main results expectedJune 2027
Study endsJune 2028
Registry record updatedJanuary 26, 2026
Trial IDNCT00710112 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are infants born weighing less than 1500 grams.

Probably not a fit

Patients with congenital heart disease (other than patent ductus arteriosus) or major congenital anomalies of the GI tract, respiratory tract, or kidneys may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to explore the relationship between genetic variations and the susceptibility to chronic lung disease (CLD) and other complications in very low birth weight (VLBW) infants. It focuses on understanding how specific gene variants, particularly those related to toll-like receptors, may influence the risk of developing conditions such as necrotizing enterocolitis, sepsis, and intraventricular hemorrhage. Additionally, the study will assess whether certain biomarkers in serum can help identify infants at higher risk for these diseases. By examining the interplay of genetic factors and biomarkers, the research seeks to provide insights into the pathogenesis of these serious conditions in premature infants.

Why it matters

Potential benefit: If successful, this study could lead to improved risk assessment and targeted interventions for premature infants at risk of chronic lung disease and other complications.

How similar studies have gone: Previous studies have indicated a correlation between genetic variants and increased risk of chronic lung disease in premature infants, suggesting that this approach has potential based on existing evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Infants born weighing less than 1500 grams

Exclusion Criteria:

* Infants born with congenital heart disease (other than patent ductus arteriosus)
* major congenital anomalies of the GI tract, respiratory tract, or kidneys

Where it's running

  • Children's Wisconsin
    Milwaukee, Wisconsin, United States
    Recruiting

Study contacts

  • Principal investigator: G. Ganesh Konduri, MD — Medical College of Wisconsin
  • Study coordinator: G. Ganesh Konduri, MD
  • Email: gkonduri@mcw.edu
  • Phone: 414.266.6820

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.