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The effect of fospropofol disodium for induction and maintenance of general anesthesia in kidney transplant patients

The effect of fospropofol disodium for induction and maintenance of general anesthesia in kidney transplant patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600115888
Enrollment
Unknown
Registered
2026-01-03
Start date
2026-01-03
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Kidney transplant

Interventions

Cipropofol group, Group C:Anesthesia induction: Cisapride 0.4 mg/kg IV Anesthesia maintenance: propofol 0.3~1.0 mg·kg-1·h-1 IV,with BIS maintained at 40-60 during the operation.
Fospropofol disodium group, Group F:Anesthesia induction: Fospropofol disodium 20 mg/kg IV
Anesthesia maintenance: Fospropofol disodium 0.3~1.0 mg·kg-1·h-1 IV,with BIS maintained at 40-60 during the operation.
Propofol group, Group P:Anesthesia induction: Propofol 2 mg/kg IV
Anesthesia maintenance: Propofol 4~12 mg·kg-1·h-1 IV,with BIS maintained at 40-60 during the operation.

Sponsors

The Second Affiliated Hospital of Guangxi Medical
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Patients undergoing their first cadaveric kidney transplantation; (2) Gender unrestricted, ASA classification III–IV, aged 18–60 years; (3) BMI 18–30 kg/m^2; (4) Regular preoperative dialysis treatment; (5) Capable of comprehending the study's procedures and methodologies, willing to sign the informed consent form, and strictly adhering to the clinical research protocol to complete the study.

Exclusion criteria

Exclusion criteria: (1) Suffering from liver, mental and nervous system diseases; (2) Coagulation dysfunction, heart failure, 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
Mean arterial pressure, Heart rate;

Secondary

MeasureTime frame
Urea, creatinine, cystatin C, glomerular filtration rate;

Countries

China

Contacts

Public ContactWu Jiangdong

The Second Affiliated Hospital of Guangxi Medical University

jiangdong020@163.com+86 188 7877 7823

Outcome results

None listed

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