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Study of glutathione combine with vitamin C preconditioning to reduce hepatic ischemia-reperfusion injury after subtotal liver resection

Study of glutathione combine with vitamin C preconditioning to reduce hepatic ischemia-reperfusion injury after subtotal liver resection

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041840
Enrollment
Unknown
Registered
2021-01-07
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-03-30

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

Conditions

Hepatic ischemia reperfusion injury

Interventions

experimental group:Pretreatment with glutathione and vitamin C
control group:Pretreatment with physiological saline

Sponsors

Taizhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Preoperative diagnosis was liver malignant tumor, liver benign tumor, intrahepatic bile duct stones, liver trauma, liver abscess, hepatic echinococcosis, etc., with surgical indications (2) The American society of anesthesiologists (ASA) classification for I/ II level (3) Subtotal liver resection is expected; According to the Quinade liver segmentation method, the resection range was not less than one liver segment. During the operation, the bleeding was controlled by the hepatic portal blood flow blocking method (Pringle method). The maximum time of each block was 15min, and the bleeding could be blocked again after the intermittent release of 5min.

Exclusion criteria

Exclusion criteria: (1) Severe underlying disease or organ failure or infection; (2) Anticoagulants or antiplatelet agents have been used before surgery; (3) Use of hormones, statins, pioglitazone, dextrometomidine and other drugs that have been reported to have similar effects of target drugs within one week before surgery; (4) Other blood flow blocking methods were also applied during the operation; (5) Due to various reasons, the acquisition of observation indicators is not perfect or surgery is not performed as planned.

Design outcomes

Primary

MeasureTime frame
glutamic-pyruvic transaminase;glutamic oxalacetic transaminase;total bilirubin;superoxide dismutase;catalase;White blood cell count;Neutrophil count;C-reactive protein;platelet;prothrombin time;Hospital stay;

Countries

China

Contacts

Public ContactChanghe Zhang

Taizhou People's Hospital

zhangchanghetz@163.com+86 15852965000

Outcome results

None listed

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