Liver Ischemia-reperfusion Injury and Clinical Data Analysis
Research on the Molecular Mechanisms of Liver Ischemia-reperfusion Injury and Clinical Data Analysis: an Observational Study
1 other identifier
observational
270
1 country
1
Brief Summary
Searching for new targets for the diagnosis and treatment of liver ischemia-reperfusion injury.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 6, 2023
CompletedStudy Start
First participant enrolled
October 10, 2023
CompletedFirst Posted
Study publicly available on registry
October 12, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2024
CompletedApril 10, 2024
April 1, 2024
2 months
October 6, 2023
April 8, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Length of hospital stay
Length of hospital stay
7days
Interventions
No intervention
Eligibility Criteria
Criteria for liver ischemia-reperfusion injury patients: patients undergoing elective liver resection surgery with hepatic pedicle occlusion and reperfusion during the procedure.
You may qualify if:
- Willingness to participate in the study and has signed an informed consent form. 2) Age ≥ 18 years and ≤ 70 years. 3) ASA classification ≤ III. 4) Criteria for liver ischemia-reperfusion injury patients: patients undergoing elective liver resection surgery with hepatic pedicle occlusion and reperfusion during the procedure.
You may not qualify if:
- \) Patients with adverse events during surgery. 2) Patients in the end stage of disease with liver failure. 3) Liver tumor metastasis with concomitant severe heart failure or chronic renal insufficiency, etc. 4) Deemed unsuitable for participation in the study based on the judgment of the researchers.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Qin Zhanglead
Study Sites (1)
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, 430030, China
Biospecimen
During the procedure, the remaining blood samples are checked for blood gas analysis, and then plasma is taken
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- phd
Study Record Dates
First Submitted
October 6, 2023
First Posted
October 12, 2023
Study Start
October 10, 2023
Primary Completion
December 20, 2023
Study Completion
September 30, 2024
Last Updated
April 10, 2024
Record last verified: 2024-04