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Effect of Different Excipients of Propofol on Plasma Lipid and Hepatic Function in Periampullary Carcinoma Patients Undergoing Whipple Procedure with general anesthesia

Clinical study of the infusion of differnt concentration MCT/LCT propofol's effect on Plasma Lipid and Hepatic Function in Patients Undergoing Whipple Procedure with general anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002627
Enrollment
Unknown
Registered
2012-10-18
Start date
2012-11-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Changes of Plasma Lipid and Hepatic Function

Interventions

Study group:2%MCT/LCT propofol
Control group:1%MCT/LCT propofol

Sponsors

The Anesthesiology Department of Beijing ChaoYang Hospital Affiliated to Capial Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Periampullary carcinoma patients will conduct Whipple procedure; 2. 18-75 years, male or female; 3. ASA I-III; 4. BMI 18.5-30; 5. Have signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients allergic to components of propofol MCT/LCT or propofol LCT, soya or peanut; (2) Pregnant or lactating women; (3) Patients with alcohol or drug abuse; (4) Patients with mental disorders or epilepsy; (5) Patients with with renal dysfunction, SCr >1.2mg/dl; (6) Cardiac dysfunction, NYHA III-IV; (7) Patients with a tumor unsectable; (8) Patients have used propofol within 1 month; (9) Patients have participated in other clinical trials within 3 months.

Design outcomes

Primary

MeasureTime frame
Plasma triglyceride (TG) concentration;

Secondary

MeasureTime frame
liver function;Plasma lipid parameters;kidney function(SCr BUN);Routine blood test;serum potassium;blood glucose;

Countries

China

Contacts

Public ContactYue Yun
yueyun@hotmail.com+86 10 85231463

Outcome results

None listed

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