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Study identifier: NCT07561125 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Bronchopulmonary Dysplasia  ·  Sponsor: International Peace Maternity and Child Health Hospital

PhasePhase 2
Planned participants29
Who can joinAll sexes, 1 Day to 10 Weeks
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Fu Xuemei  ·  +86 18017313931  ·  fxmzj2004@163.com

Li Dan  ·  +86 18814100771  ·  lidan910327@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

International Peace Maternity and Child Health HospitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07561125