Effects of Ciprofol on Myocardial Injury After Non-cardiac Surgery in Video-Assisted Thoracoscopic Surgery

Recruiting Phase 4 Interventional Study
Myocardial Injury Thoracic Diseases Thoracoscopic Surgery
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
40 – 80
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Prevention
Participants needed
1,058 (estimated)
Sponsor
Tongji Hospital · Other
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About This Trial
Myocardial injury after noncardiac surgery (MINS) refers to postoperative elevation of cardiac troponin (cTn) levels caused by underlying ischemic mechanisms (i.e., coronary artery supply-demand imbalance or atherosclerotic thrombosis) without obvious non-ischemic causes (such as pulmonary embolism), with at least one cTn concentration exceeding the 99th percentile of the test reference upper limi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Scheduled for elective video-assisted thoracoscopic (VATS)-assisted thoracic surgery (lobectomy, segmentectomy, wedge resection of two or more lung tissues, mediastinal tumor resection) under general anesthesia; 2. Aged 45 to 80 years (inclusive) at the time of randomization;…
Contacts

Ailin Luo, MD&PhD

13507122565

alluo@tjh.tjmu.edu.cn

CONTACT

Shiyong Li, MD&PhD

15002780081

shiyongli@hust.edu.cn

CONTACT