Biopsy needle showdown: which tool gets the best tissue sample?
NCT ID NCT02872831
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to compare two different needles used to take tissue samples from solid masses in the pancreas and digestive tract. The goal was to see which needle provides a more accurate diagnosis. The study was planned for adults needing this procedure, but it was withdrawn before any participants were enrolled.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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.
- Started
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Jul 2016
- Finished
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Nov 2017
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Eligible patients will include anyone \>18 years old that presents to the participating clinical institutions and requires an endosonographic evaluation for the presence of a solid-appearing mass lesion amenable to EUS access, and no contraindication to FNA as determined by standard clinical care Exclusion Criteria: 1. Refusal to participate in the study 2. Solid-appearing mass lesion that in not amenable to EUS guided needle access for tissue acquisition 3. Patients with incomplete medical records 4. Pregnant patients 5. Prisoners 6. INR \> 1.5 7. Platelets \< 50,000
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, 19107, United States
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Other studies related to the condition(s) this trial covers.
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