Neurological Sequelae in Patients With Acute Carbon Monoxide Poisoning

Jilin University

Status

Not yet enrolling

Conditions

Carbon Monoxide Poisoning

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04925297

AF-IRB-030-06

Details and patient eligibility

About

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

Full 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.

Enrollment

1,250 estimated patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

patients present within 12 hours after acute carbon monoxide poisoning;
age older than 16 years.

Exclusion criteria

pregnant women；
patients receive oxygen therapy before presentation;
have history of acute carbon monoxide poisoning within 1 year;
have been diagnosed any of the following disease: Parkinson disease; cognitive disorder, psychiatric disorders, sequelae of cerebral infarction or hemorrhage, chronic kidney disease and receive hemodialysis, congestive heart failure ( NYHA class III-IV)