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New biopsy technique could spare patients from major surgery

NCT ID NCT01892501

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study looked at whether combining a PET scan with an endoscopic ultrasound-guided needle biopsy can accurately diagnose suspicious lymph nodes in the chest. Researchers tested this less invasive approach in 75 patients who had abnormal lymph nodes on PET scans. The goal was to see if this method could replace more invasive surgical biopsies and help guide treatment decisions.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Endoscopic ultrasound-guided needle biopsy (EUS-guided puncture)
What this could lead to
If successful, this approach could provide a less invasive way to diagnose cancer in chest lymph nodes, reducing the need for more risky surgical biopsies.
What could go wrong
This is a small, early feasibility study with only 75 participants, so results may not apply to everyone. The technique may not be accurate enough to replace standard methods, and there is a small risk of complications from the biopsy.

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

75 people

The number who actually took part.

Started

Jan 2013

Finished

Oct 2019

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: 1. Any patients who have had PET showing one or more hypermetabolic lymphadenopathy in middle mediastinum and/or lower and/or posterior, and requiring diagnostic certainty for support. 2. PET scans performed in these particulars : * Pre-treatment assessment of thoracic or extra-thoracic malignancies (patients without a history of cancer). * Evaluation of response to treatment referred to oncological. * Suspicion of relapse in patients with a personal history of thoracic or extra-thoracic malignancies. 3. PET, the result is positive : * For above-centimeter lymph node short axis: greater result than or equal to the background hepatic noise. * For sub-centimeter lymph node small axis : greater result than the background hepatic noise 4. Patient with indication of diagnostic procedure surgically (whether realized or not) 5. Lymph node(s) available(s) puncture by EUS esophageal, so for a technically feasible for esophageal puncture (without vascular recusants structures) 6. Age ≥ 18 years. 7. PET scan performed within 6 weeks before EUS 8. Platelets ≥ 70 000/mm3; TP ≥ 60%. 9. Patient of childbearing age with negative pregnancy test and / or a contraception. 10. Patient gave informed consent signed. 11. Patient affiliated to a social security scheme. Exclusion Criteria: * Contra-indication (s) Director (s) to achieve a EUS. * Balance adverse anesthetic (not allowing a general anesthetic). * Esophageal stenosis. * Coagulation disorders. * Pregnant or lactating women. * Unable to undergo medical monitoring test for geographical, social or psychological reasons. * Private patient freedom and major subject of a measure of legal protection or unable to consent.

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Insitut Bergonie

    Bordeaux, Grionde, 33076, France