CClinicalTrials.gg
CompletedNCT07125612Updated Aug 15, 2025

Impact of Perioperative Allogeneic Red Blood Cell Transfusion on Postoperative Myocardial Injury After Liver Resection

An observational study in Myocardial Injury and Acuter Kidney Injury, sponsored by Hao Li. Completed. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2025-08-15.

Sponsored by Hao Li · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
487
Ages
65 Years and older
Sex
All
01

Study summary

We aimed to explore the influence of ABT on the incidence of MINS, AKI, and overall prognosis among advanced-age HCC patients who underwent hepatectomy

02

Conditions studied

  • Myocardial Injury
  • Acuter Kidney Injury

Keywords

  • perioperative allogeneic red blood cell transfusion
  • elderly surgical patients
03

In context

Lead sponsor

Hao Li is the lead sponsor of 4 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

age ≥65 years old patients

Inclusion criteria

Patients over 65 years with HCC undergoing elective surgery between January 2016 and December 2018

Exclusion criteria

Exclusion Criteria:

ASA grade V requiring repeat surgery within 1 week losing to follow-up and/or those with >5% missing data

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
487 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. the incidence of MINS within postoperative 30 days

    Time frame: postoperative day 1-30

Secondary outcomes

  1. overall survival (OS)

    the time from the date of surgery to the date of death

    Time frame: postoperative day 1-30

  2. postoperative 7-day AKI

    Time frame: postoperative day 1-7

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 15, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07125612
Lead sponsor
Hao Li
Responsible party
Hao Li (Professor, Chinese PLA General Hospital) — Sponsor-investigator
First posted
Aug 15, 2025
Start date
Jan 1, 2016
Primary completion
Dec 31, 2018
Completion
Jun 1, 2025
Last update
Aug 15, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion