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Quick pause before liver surgery may shield organ from damage

NCT ID NCT00908245

Knowledge-focused Sponsor: Assistance Publique - Hôpitaux de Paris Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a technique called ischemic preconditioning (IPC) in 81 adults having major liver surgery. Before the main operation, surgeons briefly stopped blood flow to the liver to see if it would reduce liver injury. The goal was to lower liver enzyme levels after surgery, which indicate less damage.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

81 people

The number who actually took part.

Start date

Sep 2003

Finished

Dec 2008

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * patients' age ≥ 18 years old, * liver resection of 3 segments (as described by Couinaud) or more, * posterior lesionectomy (segment VI and VII), * liver resection only or associated with a primary digestive or biliary tumor. * Portal vein embolisation allowed Exclusion Criteria: * Patients with cirrhosis, * synchronous radiofrequency or cryotherapy ablation, * undergoing segmentectomy, * left lateral lesionectomy or laparoscopic liver resection, * pregnant women

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Conditions

The condition(s) this trial relates to.

liver and intrahepatic bile duct neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Ischaemic type biliary lesion

Contacts and locations

Locations

  • Hopital Cochin

    Paris, 75014, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.