Investigating furosemide treatment strategies for severe bronchopulmonary dysplasia in infants

Furosemide in severe bronchopulmonary dysplasia: comparative effectiveness of a duration and dosage informed treatment strategy

NIH-funded research Children's Hosp of Philadelphia · NIH-10893331

This study is looking at how different amounts and lengths of a medicine called furosemide can help improve the health of premature babies with a serious lung condition called bronchopulmonary dysplasia (BPD).

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionChildren's Hosp of Philadelphia NIH-funded
Lab location1 site (Philadelphia, United States)
Project IDNIH-10893331 on NIH RePORTER

What this research studies

This research focuses on improving treatment strategies for infants suffering from severe bronchopulmonary dysplasia (BPD), a serious lung condition often seen in premature babies. The study aims to evaluate the effectiveness of different dosages and durations of furosemide, a diuretic medication, to enhance outcomes for these vulnerable patients. By utilizing a patient-oriented approach, the research will gather data on how these treatment strategies impact the health and recovery of infants with severe BPD. The project also emphasizes mentorship and training for the lead investigator to foster future independent research in pediatric care.

Who could benefit from this research

Good fit: Ideal candidates for this research are premature infants diagnosed with severe bronchopulmonary dysplasia.

Not a fit: Patients who are not premature or do not have a diagnosis of severe bronchopulmonary dysplasia may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could lead to more effective treatment protocols for infants with severe bronchopulmonary dysplasia, potentially improving their long-term health outcomes.

How similar studies have performed: Previous research has shown promising results with similar treatment strategies for bronchopulmonary dysplasia, indicating potential for success in this approach.

Where this research is happening

Philadelphia, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-10 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.