New Angle-Measuring tools could make biopsies more accurate
NCT ID NCT01218854
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested two simple tools—a laser pointer and a plastic block—to help doctors pick the correct angle for inserting a biopsy needle during CT scans. Seventeen adults scheduled for a CT-guided biopsy took part. The goal was to see if these tools improved angle selection compared to the usual method of estimating by experience. No actual biopsies were performed using the tools; only the needle angle was measured.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, these guidance methods could make biopsies more accurate and reduce the need for repeat procedures.
- What could go wrong
- This was a very small, early-phase study (17 people) that only measured needle angle, not actual biopsy success. The methods may not improve outcomes in real procedures.
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
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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17 people
The number who actually took part.
- Started
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Mar 2012
- Finished
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Nov 2016
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
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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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 Hide 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 must fulfill all of the following criteria to be eligible for study admission: * All patients must be undergoing a CT-guided biopsy. * Age greater than 18 years. * No serious concurrent medical illness that would preclude the patient from making a rational informed decision on participation. * The ability to understand and willingness to sign a written informed consent form, and to comply with the protocol. If in question, an ethics consult will be obtained. * Ability to follow breathing instructions like holding breath (if procedure is to be performed without general anesthesia). * Patients must be actively enrolled on an NIH protocol and be scheduled for a CT-guided biopsy. EXCLUSION CRITERIA: * Patients with an altered mental status that precludes understanding or consenting for the biopsy procedure will be excluded from this study. * Patients unlikely to be able to hold reasonably still on a procedure table for the length of the procedure. * Patients with any known allergy to plastics or polymers (since the Ultem -polymer could theoretically induce a rash in these patients, even though it is hypoallergenic). * Inability to follow breathing instructions, if without general anesthesia. * Patients with pacemakers or automatic implantable cardiac defibrillators. * Gross body weight above the CT table limit (450 pounds).
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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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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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