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Effects of different anesthetics and analgesics on perioperative cardiovascular function and myocardial protective homeostasis in patients with intravenous general anesthesia

Effects of different anesthetics and analgesics on perioperative cardiovascular function and myocardial protective homeostasis in patients with intravenous general anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037952
Enrollment
Unknown
Registered
2020-09-06
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

General anesthesia

Interventions

Opioid analgesic group:Use opioids analgesic for analgesia
Esmolamine group:Use of esmolamine for analgesia

Sponsors

The Second Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with informed consent; 2. Patients undergoing elective noncardiac surgery under general anesthesia; 3. ASA I-III patients; 4. Patients aged 20-75 years.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications of general anesthesia; 2. Patients who are allergic or intolerant to ketamine hydrochloride, esketamine hydrochloride, propofol, rocuronium, opioids, neostigmine and belladonna alkaloids; 3. Patients who have used narcotic analgesics within 24 hours or within 5 days; long-term (continuous or intermittent) use of benzodiazepines and opioids; 4. Patients with abnormal coagulation function (Pt or r-inr > 1.5 ULN, APTT >1.5 ULN) have bleeding tendency (such as active gastrointestinal ulcer) or are receiving thrombolytic or anticoagulant therapy; 5. Anemia or thrombocytopenia, PLT =1.5 ULN, TBIL >=1.5 ULN; 7. In patients with abnormal renal function, bun >= 1.5 ULN and creatinine exceeding the upper limit of normal value; 8. Patients with a history of serious cardiovascular diseases (such as myocardial ischemia, cardiac dysfunction, arrhythmia, etc.); angina pectoris (unstable angina pectoris) due to insufficient coronary artery blood supply, or myocardial infarction in recent 6 months; 9. Patients with hypertension whose blood pressure has not been controlled satisfactorily by using antihypertensive drugs (SBP >=160 mmHg and / or DBP >=100mmhg); 10. Patients with craniocerebral injury, possible high intracranial pressure, cerebral aneurysm, cerebrovascular accident disease history and other central nervous system diseases; 11. Patients with diabetes whose blood glucose was not controlled satisfactorily (blood glucose >=11.1 mmol/L); 12. Patients with a history of drug abuse and / or alcoholism within 2 years; alcoholism, i.e. drinking more than 2 units of alcohol per day on average, (1 unit of alcohol = 360ml of beer or 150 ml of 45 ml of strong liquor with 40% alcohol content); 13. Pregnant or lactating women; 14. Patients with hyperthyroidism and / or history of hyperthyroidism; 15. Patients with a history of high intraocular pressure (e.g. glaucoma) or penetrating eye injury; 16. Patients with abnormal lipid metabolism, including primary hyperlipidemia, diabetic hyperlipidemia and pancreatitis; 17. Patients with mental illness and / or history (including schizophrenia, mania, bipolar disorder, mental disorder, etc.) and the use of psychotropic drugs, i.e. cognitive impairment; 18. Patients with asthma disease and / or history; 19. Patients with difficult airway (modified Mahalanobis score was grade IV); 20. Patients who have received clinical trials of drugs in the past three months; 21. Patients considered unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
Abnormal hemodynamic fluctuations;Arrhythmia;Myocardial ischemia;miocardial infarction;Acute heart failure;Cardiac arrest;TRPV1 content;CGRP content;SP content;cTnI content;

Secondary

MeasureTime frame
Drug dosage;Blood loss;Urine volume;fluid replacement volume;NRS pain score;Restlessness score;Determination of recovery time of directional force;

Countries

China

Contacts

Public ContactGuo Zheng

The Second Hospital of Shanxi Medical University

Guozheng713@yahoo.com+86 13603566922

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026