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Could a quick ultrasound replace painful liver biopsies for kids?

NCT ID NCT01072721

Diagnosis 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether a noninvasive device called FibroScan can accurately measure liver scarring (fibrosis) in children, potentially replacing the need for a liver biopsy. Researchers compared FibroScan results with biopsy results in 264 children aged 6 months to 18 years with various liver diseases. If proven effective, this could make diagnosis and monitoring much easier and less painful for young patients.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

264 people

The number who actually took part.

Started

Jan 2010

Finished

Apr 2018

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

6 months to 18 years

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 : * Children age more than 6 months and under 18 years old. * Children with an hepatic biopsy for any fibrosis hepatitic diseases * Clinical examination by a physician Exclusion criteria : * Children of less than 6 months and more than 18 years old. * Pregnant women. * No written informed consent * No social security

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Conditions

The condition(s) this trial relates to.

cirrhosis of liver cystic fibrosis Fibrosis fibrotic liver disease parenteral nutrition-associated cholestasis portal hypertension

As listed by the trial registrant

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

Cholestasis of parenteral nutrition Cirrhosis Cystic fibrosis Liver fibrosis Portal hypertension

Contacts and locations

Locations

  • Necker Hospital

    Paris, 75015, France

More trials for these conditions

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