Comparing feeding methods in preterm infants on non-invasive ventilation

Is this trial a fit for you?

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

What this trial studies

This study evaluates the effectiveness of continuous versus bolus feeding methods in preterm infants receiving non-invasive respiratory support. Preterm infants aged 24-34 weeks will be randomly assigned to either continuous nasogastric feeding or intermittent bolus feeding. The goal is to determine which feeding method allows infants to reach full feeds more quickly. Parents will provide consent, and the study will be conducted in a Level III Neonatal Intensive Care Unit.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Preterm Infants 24- 34 weeks of gestation
2. On Non-invasive ventilation (NIPPV/CPAP/HFNC)
3. Nothing by mouth (NPO) or on trophic feeds (\<20 ml/kg/day) at the time of randomization.

Exclusion Criteria:

1. Gestational Age \> 34 weeks
2. Infants on invasive ventilation or low flow nasal cannula and on feeding volume more than trophic feeds.
3. Major congenital anomalies.

Where it's running

• Cook County Helath
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: Rajeev Kumar, MD — Cook County Health
• Study coordinator: Aashika Janwadkar, MD
• Email: aashika.janwadkar@cookcountyhealth.org
• Phone: 6469343483

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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.