This study aims to evaluate the clinical efficacy of Danhong injection in patients with septic myocardial injury through a prospective randomized controlled trial. The study will enroll 140 patients meeting criteria for septic myocardial injury, divided into a Danhong injection group and a placebo group. Primary endpoints include changes in myocardial injury markers and improvement rates in cardiac function over 7 days, while secondary endpoints include 28-day mortality rates. This will determine whether Danhong injection possesses myocardial protective effects and provide evidence-based support for expanding its clinical indications.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
140
Danhong Injection for intravenous drip, dosage: 20 ml, diluted in 80 ml of 0.9% saline solution for intravenous drip, twice daily, for a continuous treatment period of 7 days.
Intravenous drip of 100 ml 0.9% saline solution, twice daily, for 7 consecutive days.
Left Ventricular Ejection Fraction
Time frame: 24 hours before treatment, 3 days after treatment
cardiac troponin T
Time frame: Before treatment, 3 days after treatment, 7 days after treatment
28-day mortality
Time frame: 28 days after enrollment
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