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NCT02983903 · ClinicalTrials.gov registry record · NA

Cryobiopsy Versus Forceps Biopsy for Pulmonary Lesions

A NA study, sponsored by University of Pennsylvania.

Terminated
Registry status
NA
Development phase
31
Enrollment target

NCT02983903: Clinical Trial NA study, sponsored by University of Pennsylvania.

NCT02983903 is a NA study that was terminated before completion, run by University of Pennsylvania. The registered enrollment target is 31 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02983903, a NA study, was terminated before completion, sponsored by University of Pennsylvania.

TERMINATED
Registry status
NA
Development phase
31 participants
Enrollment target

Study Summary

Purpose: Patients with peripheral lung nodules require evaluation for lung cancer. Our aim is to assess the diagnostic yield of a new technique, transbronchial cryobiopsies, in patients at risk for lung cancer. Target population: Patients referred for bronchoscopy and lung biopsies as a part of their work up for peripheral lung lesions. Procedures: Patients enrolled will have forceps transbronchial biopsies followed by transbronchial cryobiopsies for their lung lesion during bronchoscopy.

Primary Outcome

Sensitivity for cancer is defined as true positives / (true positives + false negatives) with respect to diagnosing malignancy. If the bronchoscopic procedure fails to diagnose malignancy, the gold standard will be the results of any further, more invasive testing that is clinically indicated to evaluate the nodule.

Interventions

  • PROCEDURE transbronchial biopsy

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2016-11
Est. Completion 2020-03-02
Phase NA
University of Pennsylvania

1,423 total trials

Why NCT02983903 stopped before completion

NCT02983903 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which transbronchial biopsy is the first listed.

NCT02983903 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02983903 about?

NCT02983903 is a clinical study titled "Cryobiopsy Versus Forceps Biopsy for Pulmonary Lesions". Purpose: Patients with peripheral lung nodules require evaluation for lung cancer. Our aim is to assess the diagnostic yield of a new technique, transbronchial cryobiopsies, in patients at risk for lung cancer. Target population: Patients referred for bronchoscopy and lung biopsies as a part of thei...

What is the current status of trial NCT02983903?

This trial is currently terminated. It is a NA study. The enrollment target is 31 participants. The study started on 2016-11. Estimated completion is 2020-03-02.

What interventions are being tested in trial NCT02983903?

The interventions under investigation include: transbronchial biopsy (PROCEDURE).

Who is sponsoring clinical trial NCT02983903?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02983903's enrollment target sits among peer trials

31 1592nd of 2000 higher than 408 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02983903, the US trial registry maintained by the National Library of Medicine. NCT02983903 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.