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Clinical Trial Summary

The purpose of this study is to access the clinical characteristics and risk factors for neurological sequelae after acute carbon monoxide poisoning.


Clinical Trial Description

After being informed about the study and potential risks, patients meet the inclusion criteria would be given informed consent and entry the study. The data will be collected according to self-designed questionnaire, including :1) The baseline characteristics: would be recorded 6 hours after patients presentation;2) Patients' self evaluation for discomfort symptoms: would be recorded at day 0, week 1, 3 and 6, month 6 and 12;3) Neurological function: would be recorded at day 0, week 6, month 6 and 12. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04925297
Study type Observational [Patient Registry]
Source The First Hospital of Jilin University
Contact Ning Dong, M.D.
Phone +8615804301769
Email dnjl2007@jlu.edu.cn
Status Not yet recruiting
Phase
Start date August 1, 2021
Completion date May 1, 2027

See also
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