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Search / Trial NCT07019246

Safety of Etomidate-propofol Mixture vs. Propofol for Total Intravenous Anesthesia in Elderly Patients Undergoing Abdominal Surgery

Launched by TONGJI HOSPITAL · Jun 12, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at the safety of a combination of two medications, etomidate and propofol, compared to using propofol alone for total intravenous anesthesia in older patients who are having abdominal surgery. The goal is to see which option is safer for this age group, which is particularly important because older patients may have different health needs and risks.

To be eligible for the trial, participants should be between 65 and 80 years old, have a body mass index (BMI) between 18 and 28, and be scheduled for an elective surgery that will require anesthesia lasting between 1 to 4 hours. However, people with certain health issues—like severe high blood pressure, recent heart problems, uncontrolled diabetes, or significant liver and kidney problems—will not be able to participate. If you or a loved one is considering joining this study, you can expect to receive carefully monitored anesthesia during your surgery and help researchers learn more about how to keep older patients safe during these procedures.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • ASA Ⅰ\~Ⅲ;
  • BMI was 18-28 kg/m2;
  • For elective abdominal surgery under intravenous general anesthesia;
  • The expected duration of anesthesia was 1 to 4 hours.
  • Exclusion Criteria:
  • Septic shock and multiple organ failure diagnosed within 14 days;
  • Hyperkalemia (serum potassium \>5.5mmol/L) within 48 hours;
  • Stroke or transient ischemic attack within 3 months;
  • Patients with unstable angina pectoris or myocardial infarction within 3 months; Arrhythmia requiring treatment was not treated or treatment did not meet expectations;
  • Patients with preoperative diagnosed diabetes mellitus and uncontrolled blood glucose; Diabetic complications were diagnosed before surgery, including diabetic ketoacidosis, hyperosmolar coma, diabetes-related infection, diabetic nephropathy, retinopathy, diabetic cardiomyopathy, diabetic neuropathy, diabetic foot, etc.
  • Severe liver and renal dysfunction;
  • Liver surgery, renal surgery, adrenal surgery, day surgery;
  • Resting blood pressure ≥180/110 mmHg (2020 ISH hypertension guideline ≥ grade 3 hypertension); Or systolic blood pressure \<90mmHg or mean blood pressure \<65mmHg.
  • Taking corticosteroids or other immunosuppressants for more than 10 days within 6 months or having a history of adrenal cortex suppression or immune system diseases;

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, Hubei, China

Patients applied

0 patients applied

Trial Officials

Shiyong Li

Principal Investigator

Department of Anesthesiology of Tongji Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported