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The randomized controlled clinical sudy on preventive effects of N-acetylcysteine on hepatic ischemia reperfusion injury

The randomized controlled clinical sudy on preventive effects of N-acetylcysteine on hepatic ischemia reperfusion injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034221
Enrollment
Unknown
Registered
2020-06-28
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

liver cancer

Interventions

control group:Normal saline

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Preoperative diagnosis of liver cancer, no portal vein trunk involvement, no distant metastasis, elective partial hepatectomy; (2) Older than 15 years and younger than 75 years (including 15 and 75 years); (3) Liver and kidney function was basically normal, without obvious complications of heart, lung, kidney and other important organs; liver function was child-A/B grade and ASA grade I-III; (4) Drugs affecting liver function and blood coagulation system were not used before surgery; (5) Pringe method was used in intraoperative golden a hepatic blood flow barrier analysis.

Exclusion criteria

Exclusion criteria: (1) Chronic inflammatory diseases that affect the immune and metabolic system; (2) Abnormal state of coagulation function; (3) Active infection; (4) Intraoperative occlusion of total hepatic blood flow was less than 30 minutes or more than 90 minutes; (5) Other factors, such as drug allergy, are not suitable for the administration of N-acetylcysteine after evaluation by clinicians; (6) Refuse to participate in or quit the study.

Design outcomes

Primary

MeasureTime frame
Liver function;

Secondary

MeasureTime frame
Interleukin-6;Tumor necrosis factor;Interleukin-10;Superoxide dismutase;Malondialdehyde;Clinical indicators;

Countries

China

Contacts

Public ContactLiu Quanyan

Tianjin Medical University General Hospital

18071091908@163.com+86 18071091908

Outcome results

None listed

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