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UnknownNCT05372211

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
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Shenzhen People's Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERnot use of any interventionnot use of any intervention

Timeline

Start date
2022-06-01
Primary completion
2022-09-01
Completion
2022-10-01
First posted
2022-05-12
Last updated
2022-05-12

Source: ClinicalTrials.gov record NCT05372211. Inclusion in this directory is not an endorsement.