Clinical Trial

Effects of IVIG for BPD in Preterm Infant Born at 28 Weeks and Below

Recruiting Phase 2
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Summary
It is intended to examine the short-term and long-term efficacy and safety of intravenous immunoglobulin(IVIG) for the bronchopulmonary dysplasia in preterms born at 28 weeks and below. Participants will received continuous infusion IVIG 1 g/kg/day for the first 2 days, 0.5 g/kg/day for next 3 days (total does 3.5 g/kg), repeatable if necessary.
Protocol Amendment History 1 change
critical Primary endpoint(s) modified 2026-07-24
Trial Details
NCT Number NCT07561125
Lead Sponsor International Peace Maternity and Child Health Hospital
Conditions Bronchopulmonary Dysplasia
Enrollment 29 participants
Start Date 2026-04-23
Primary Completion 2027-09 (estimated)
Study Completion 2029-09 (estimated)
Updated on ClinicalTrials.gov 2026-07-23