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To Compare the Effects of Cyclopofol and Propofol on Circulatory Function in Patients with Heart Valve Replacement during Induction of General Anesthesia

To Compare the Effects of Cyclopofol and Propofol on Circulatory Function in Patients with Heart Valve Replacement during Induction of General Anesthesia

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071427
Enrollment
Unknown
Registered
2023-05-15
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Valvular disease

Interventions

Cyclopofol group:Group A: 0.3mg/kg was injected with cyclopofol pump, and 50ug of sufentanil was injected with constant speed pump. After patients fell asleep, cisatracurium was injected intravenousl
Propofol group:Group B: Target pump infusion of propofol, and 50ug of sufentanil was injected with constant speed pump. After patients fell asleep, cisatracurium was injected intravenously, and endotr

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: A. Patients undergoing elective heart valve replacement; B. ASA classification I-III; C. Age >=18 years old, male or female; D. NYHA grade II to III; E. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: A. Allergic to or contraindicated to propofol, cyclopofol, opiates and other drugs and their components; B. Severe cardiac insufficiency, ASA level ? or above; C. Abnormal liver function: ALT and/or AST exceeding 1.5 times the upper limit of the medical reference range; D Abnormal renal function: creatinine exceeding the upper limit of the medical reference range; E. Preoperatively complicated with mental disorders; F. Heart failure within one month before surgery; G. Drug and alcohol addicts; H. Patients with difficult airway: Markov grade ? or above.

Design outcomes

Primary

MeasureTime frame
Intake and exit volume;Anesthetic dosage;Vasoactive drug use;Onset time of sedatives;Pain stimulation at administration site;Intraoperative awareness;Postoperative ventilator use time;ICU stay time;Postoperative nausea and vomiting;Postoperative delirium (delirium Assessment scale);

Countries

china

Contacts

Public ContactQi Mao

The First Affiliated Hospital of Guangxi Medical University

644826829@qq.com+86 15240684649

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 28, 2026