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Effect of esketamine on prevention of hypotension induced by propofol general anesthesia

Effect of esketamine on prevention of hypotension induced by propofol general anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059304
Enrollment
Unknown
Registered
2022-04-28
Start date
2022-04-25
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Hypotension

Interventions

Experimental group:Esketamine intravenously
Control group:Propofol intravenously

Sponsors

Affiliated Cancer Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-60 years old, no gender limitation; 2. Patients undergoing elective surgery under general anesthesia and single endotracheal intubation; 3. ASA I or II; 4. 18 kg/m2 < BMI < 28kg/m2; 5. They clearly understood and voluntarily participated in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who have not received regular antihypertensive therapy or have poor blood pressure control (systolic blood pressure >=160 mmHg or =100 mmHg); 2. Sinus bradycardia, pathological sinus syndrome, and other arrhythmias. 3. Uncontrolled diabetes, coronary heart disease; 4. With central nervous system diseases; 5. Difficult airway; 6. Allergy to research drugs; 7. Discontinuous or long-term use of benzodiazepines or opioids within 2 months before admission; 8. Untreated or uncontrolled hyperthyroidism; 9. Participated in clinical trials of other drugs as a subject within the last 3 months.

Design outcomes

Primary

MeasureTime frame
Blood pressure;

Secondary

MeasureTime frame
Heart rate;The injection pain;Endotracheal intubation response;

Countries

China

Contacts

Public ContactRui Li

Affiliated Cancer Hospital of Guizhou Medical University

250352808@qq.com+86 18285123165

Outcome results

None listed

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