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A Study on the Half-Effective Dose of Disodium Propofol Phosphate for General Anesthesia Induction in Kidney Transplant Recipients

A Study on the Half-Effective Dose of Disodium Propofol Phosphate for General Anesthesia Induction in Kidney Transplant Recipients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125406
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-05-27
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Uraemia

Interventions

Experimental group:Anaesthetic induction using a sequential regimen of disodium propofol phosphate

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 65; 2. ASA physical status score: III–IV; 3. BMI 18.5–30.0 kg/m^2; 4. Performed the first kidney transplant; 5. No severe dysfunction of vital organs such as the heart, lungs or liver; 6. No neurological disorders or mental health issues; 7. No history of allergy to disodium propofol or propofol.

Exclusion criteria

Exclusion criteria: 1. Participants who do not consent to participate in this study; 2. Patients with a known allergy to disodium propofol, propofol or related components; 3. Patients with suspected difficult airway or intubation difficulties; 4. Patients with concomitant dysfunction of vital organs such as the heart, lungs, brain or liver; 5. Pregnant or breastfeeding women; 6. Patients with a history of substance abuse or dependence on long-term sedatives, hypnotics or opioids; 7. Patients requiring modification of the anesthetic plan or a change in surgical approach due to surgery-related factors; 8. Patients who have participated in other drug clinical trials within the past three months.

Design outcomes

Primary

MeasureTime frame
Observation of loss of consciousness in kidney transplant recipients following administration of a predetermined dose of disodium propofol;The correlation between ED95 during general anaesthesia-induced sedation in kidney transplant recipients and serum alkaline phosphatase levels.;

Secondary

MeasureTime frame
Record the time at which sedation was achieved and the incidence of adverse reactions in patients;On admission, prior to induction, 1 minute before intubation, and after intubation: blood pressure, heart rate and BIS.;

Countries

China

Contacts

Public ContactXie Yanhu

The First Affiliated Hospital of University of Science and Technology of China

xyh200701@sina.cn+86 181 6088 6165

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026