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Improving Outcome of Very Preterm Infants Using Collaborative Quality Improvement

Fudan University logo

Fudan University

Status

Withdrawn

Conditions

Morbidity;Newborn
Morality

Treatments

Behavioral: Evidence-based collaborative quality improvement

Study type

Interventional

Funder types

Other

Identifiers

NCT04531839
SH-EPIQ 20200826

Details and patient eligibility

About

A multicenter interventional study using evidence-based collaborative quality improvement to reduce mortality and major morbidities of very preterm infants in six neonatal centers in Shanghai

Full description

A multicenter interventional study using evidence-based collaborative quality improvement to reduce mortality and major morbidities of very preterm infants using evidence-based collaborative quality improvement interventions including benchmarking, potential better practice list, PDSA implementation and collaborative learning.

Sex

All

Ages

Under 120 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Infants born at >=24+0 weeks' gestation and <32+0 weeks' gestation;
  2. Admitted to the participating NICUs within 7 days after birth during study period

Exclusion criteria

  1. Infants with major congenital anomalies;
  2. Infants who transferred to non-participating hospitals within 24 hours after birth;

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Intervention period
Experimental group
Description:
The 1.5-year period during which all six participating centers receive evidence-based collaborative quality improvement interventions including benchmarking, potential better practice list, PDSA implementation, and collaborative learning
Treatment:
Behavioral: Evidence-based collaborative quality improvement
Baseline period
No Intervention group
Description:
The 2-year period before the collaborative quality improvement intervention

Trial contacts and locations

6

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Central trial contact

Yun Cao, MD,PHD

Data sourced from clinicaltrials.gov

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