Skip to content

Intraoperative haemodynamic effects of cyclopentol and propofol in renal transplant patients

Intraoperative haemodynamic effects of cyclopentol and propofol in renal transplant patients

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081018
Enrollment
Unknown
Registered
2024-02-20
Start date
2023-06-11
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

End stage renal disease

Interventions

Control group:Propofol

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Those who underwent cadaveric kidney transplantation; 2. There is no restriction on gender, ASA grade III ~ IV, age 18 ~ 65 years old; 3. Dialysis was performed regularly before the operation; 4. Be able to understand the procedures and methods of this study, be willing to sign the informed consent, and strictly abide by the clinical research protocol to complete this study.

Exclusion criteria

Exclusion criteria: 1. Suffering from liver, mental and nervous system diseases; 2. Coagulation dysfunction, heart failure, and respiratory failure; 3. Long-term use of sedative or antidepressant drugs; 4. Pregnant or lactating women; 5. Unable to communicate and cooperate.

Design outcomes

Primary

MeasureTime frame
Cardiac output(CO);

Secondary

MeasureTime frame
Stroke volume(SV);Systemic vascular resistance(SVR);

Countries

China

Contacts

Public ContactXueke Du

The Second Affiliated Hospital of Guangxi Medical University

46699644@qq.com+86 173 0771 1159

Outcome results

None listed

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