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Protective Effect of propofol postconditioning on liver transplant patients

Clinical research on protective effect of propofol postconditioning in liver transplant patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003232
Enrollment
Unknown
Registered
2013-04-19
Start date
2013-06-01
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

end-stage liver disease

Interventions

Experimental group:propofol postconditioning
Control:not treated by propofol postconditioning

Sponsors

Department of Anesthesiology in the Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) >18 years of age; (2) can be acquired informed consent; (3) without any other diagnostic organ dysfunction;who are scheduled for allogeneic orthotopic liver transplantation.

Exclusion criteria

Exclusion criteria: (1) >65 years of age; (2) cannot be acquired informed consent; (3) are accompanied with other diagnostic organ dysfunction; (4) need any other operation together except liver transplantation; (5) have massive haemorrhae (>10000ml) during the surgery.

Design outcomes

Primary

MeasureTime frame
perioperative adverse events;duration time of ICU;survival rate in half year, 1 and 3 year;pathologic change;expression of Nrf2, Brg1 and antioxidase;liver function;

Countries

China

Contacts

Public ContactHei Ziqing
heiziqing@sina.com+86 13925020330

Outcome results

None listed

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