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Survey on the Clinical Use of Recombinant Human Erythropoietin in VLBW and ELBW Infants

Clinical Use of Recombinant Human Erythropoietin in VLBW and ELBW Infants: a National Survey in China

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05372211
Acronym
NSEPO
Enrollment
500
Registered
2022-05-12
Start date
2022-06-01
Completion date
2022-10-01
Last updated
2022-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erythropoietin; Infant; Surveys and Questionnaires

Brief summary

Recombinant human erythropoietin (rhEPO) has been shown to effectively and safely prevent the anemia of prematurity and to reduce the transfusion need in very low birth weight (VLBW) and extremly low birth weight (ELBW) infants and has been licensed for this indication in Europe in 1997. The objective of the study was to obtain information on the use or nonuse of rhEPO in neonatal units in China.

Detailed description

The survey was developed by a team of neonatologists at Shenzhen People's hospital . The survey consisted of 26 questions covering three areas: the characteristics of the survey respondents, the use of rhEPO in VLBW and ELBW infants , and other related questions. The questionnaire was presented in the Questionnaire Star format (https://www.wjx.cn/, Hangzhou Oway Medical Technology,Changsha, China). we plan to conduct a cross-sectional survey through the Neonatal Professional Committee of the Chinese Medical Doctor Association WeChat platform. The questionnaire is going to be distributed to nearly 500 representative neonatologists and pediatricians from general hospitals, maternity and infant hospitals, and children's hospitals across the country. Furthermore, this study was approved by the ethics committee of the Shenzhen People's Hospital.

Interventions

OTHERnot use of any intervention

not use of any intervention

Sponsors

Shenzhen People's Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

neonatologists and pediatricians from general hospitals, maternity and infant hospitals, and children's hospitals across China

Exclusion criteria

neonatologists and pediatricians from same hospitals

Design outcomes

Primary

MeasureTime frameDescription
The survey (the clinical use of rhEPO)01-june-2022the clinical use of rhEPO in VLBW and ELBW infants

Contacts

Primary ContactZhangbin Yu, Doctor
yuzhangbin@126.com+86 13913994139
Backup ContactXudong Yan, Master
yan-xu-dong@126.com+86 13480780053

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026