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Clinical Trial Summary

The objective of this study was to evaluate the effect of esketamine on intraoperative hemodynamics in patients with heart valve replacement and to mitigate postoperative pulmonary complications


Clinical Trial Description

After being informed of the study and potential risks, all patients who gave written informed consent will undergo pre-operative screening to determine eligibility for study enrollment. Before operation, eligible patients were randomly divided into esketamine group (0.2mg/kg, intraoperative pump), esketamine group (0.4mg/kg, intraoperative pump) and blank control group (physiological salt pump) in a double-blind way at a ratio of 1:1:1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06467513
Study type Interventional
Source Zunyi Medical College
Contact Xiaomei Zhang
Phone +0086 18786233321
Email 3233598996@qq.com
Status Recruiting
Phase Phase 4
Start date January 1, 2024
Completion date May 2025

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