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Search / Trial NCT07028593

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

Launched by TONGJI HOSPITAL · Jun 11, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Myocardial Injury After Non Cardiac Surgery Ciprofol Propofol Video Assisted Thoracoscopic Surgery Lung Tumor

ClinConnect Summary

This clinical trial is looking at whether a drug called Ciprofol can help reduce heart injury after lung surgery done with a minimally invasive technique called video-assisted thoracoscopic surgery (VATS). Heart injury after surgery, even when the surgery isn’t on the heart itself, can happen when the heart doesn’t get enough blood, which can increase risks of serious problems and even death within days or years after surgery. Since Ciprofol is known to keep the heart and blood circulation stable during anesthesia, researchers want to see if using it during these lung surgeries can lower the chances of heart injury afterward.

People who might take part are adults aged 45 to 80 who are scheduled for planned lung surgeries using VATS, such as removing part of the lung or tumors, and who expect to stay in the hospital for at least three days after surgery. Participants will receive general anesthesia during their procedure, and the study will monitor their heart health after surgery. However, people with certain health issues like severe lung disease, unstable heart conditions, allergies to the drug or its ingredients, or who are pregnant or planning to become pregnant soon, would not be eligible. This study is not yet recruiting participants but aims to improve care and safety for patients having these types of lung surgeries.

Gender

ALL

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;
  • 3. Expected postoperative hospital stay of ≥3 days;
  • 4. Signed a written informed consent to participate in the study.
  • Exclusion Criteria:
  • 1. Patients allergic to propofol, Ciprofol, or analogs of drug excipient components (soybeans, eggs, milk);
  • 2. Patients with unstable angina;
  • 3. Patients with congestive heart failure or hemodynamic instability requiring vasopressor agents;
  • 4. Patients with severe COPD (FEV1 \< 1 L);
  • 5. Glomerular filtration rate \[eGFR\] \< 30 mL/min/1.73m²;
  • 6. Patients with severe hepatic dysfunction (ALT or AST elevation exceeding 1.5 times the upper limit of normal);
  • 7. Male or female patients planning to conceive within the next 3 months;
  • 8. Pregnant or lactating female patients;

About Tongji Hospital

Tongji Hospital, affiliated with Tongji Medical College of Huazhong University of Science and Technology, is a leading medical institution in China dedicated to advancing healthcare through innovative research and clinical trials. With a robust infrastructure and a multidisciplinary team of experts, Tongji Hospital focuses on translating scientific discoveries into effective treatments and therapies. The hospital is committed to enhancing patient care by conducting rigorous clinical trials that adhere to the highest ethical and regulatory standards, fostering collaboration with both national and international research communities to drive medical advancements.

Locations

Wuhan, , China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported