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Chinese Neonatal Extracorporeal Life Support Registry (Chi-NELS)

Fudan University logo

Fudan University

Status

Withdrawn

Conditions

Neonate
Extracorporeal Life Support

Study type

Observational

Funder types

Other

Identifiers

NCT05085080
Chi-NELS

Details and patient eligibility

About

Extracorporeal life support (ECLS), also known as extracorporeal membrane oxygenation (ECMO), is an extracorporeal technique which provides respiratory and cardiac support to patients with respiratory and/or heart failure. Neonates account for a significant proportion of patients requiring ECLS support. While with unique pathophysiology among newborn infants, neonatal ECLS treatment faces different challenges (such as specific indications, anticoagulation, hemodynamic management, high incidences of complications, ect.) from those of elder children or adults. Though neonatal ECMO has been used in developed countries since 1970s, the introduction of neonatal ECMO in China was not reported until 2010s. While on the other hand, there has been a rapid increase of neonatal ECLS cases and centers in China in the past decade with a huge variation of numbers of cases and quality among different centers. Therefore, there is an urgent need to monitor the use and quality of neonatal ECLS in China. The goal of the Chinese Neonatal Extracorporeal Life Support Registry (Chi-NELS) is to maintain a registry of use of ECLS in active neonatal ECLS centers across China, to support quality improvement of neonatal ELCS, clinical research and regulatory agencies.

Full description

This study aims to establish a neonatal ECLS network of all active ECLS centers in China to facilitate standardization of care and collaborative research. On the basis of the network, this prospective comprehensive registry will enroll all neonates who receive ECLS support in participating centers. The indications, managements, complications and outcomes of neonatal ECLS in China will be described in detail, to monitor the development of neonatal ECLS in China, to identify targets for quality improvement, to assist in reducing mortality and morbidity of neonates requiring ECLS support, and to facilitate innovative clinical researches.

Sex

All

Ages

1 hour to 1 month old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≤28 days of life
  • receive ECLS support

Exclusion criteria

  • none

Trial contacts and locations

0

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Central trial contact

Yun Cao, Ph.D. M.D.; Siyuan Jiang, Ph.D. M.D.

Data sourced from clinicaltrials.gov

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