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Clinical Trial Summary

Retrospective and Prospective single arm, observational study to evaluate efficacy and safety of NIF in the treatment of ventricular tachycardia and ventricular fibrillation. The information registration of the target population will be collected with the hospital HIS system or LIS system.


Clinical Trial Description

Subjects enrolled in the retrospective study may be enrolled in a prospective study if the study drug is re-used, but in the end only the most-registered case of the subject would be collected.

The recommended treatment plan for this study is from the usage and dosage of NIF. The clinician can make appropriate adjustments to the specific usage and dosage according to the patient's condition.

Load dose: Adults usually use 0.3mg/kg each time, under continuous ECG monitoring, the injection should be completed within 5 minutes, and the maximum dose should not exceed 0.5 mg/kg.

Maintenance dose: After load injection, the adult routine dose is 0.4 mg/kg/h under continuous ECG monitoring. The dosage could be appropriately increased or decreased according to the patient's reaction, but the maximum dose should not exceed 0.8 mg/kg/h. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03853369
Study type Observational
Source Sichuan Baili Pharmaceutical Co., Ltd.
Contact Jing Xiong
Phone +86-028-85320612
Email xiongjing@baili-pharm.com
Status Recruiting
Phase
Start date February 18, 2019
Completion date December 30, 2019

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