Ethics and Data Quality

Cross-source consensus on Ethics and Data Quality from 1 sources and 5 claims.

1 sources · 5 claims

Evidence quality

The protocol was approved by the Medical Ethics Committee of Shenzhen Children’s Hospital and registered as ChiCTR2400094994. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
Written informed consent will be obtained from guardians according to the Declaration of Helsinki. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
Each participating unit will appoint an attending neonatologist as a database management specialist. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
A first-level quality controller with at least 3 years of clinical research experience will review and lock case data. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
The coordinating centre manages the online registry and data security. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study