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CompletedNot applicableNCT03523689
Official study title

Radial-Probe Endobronchial Ultrasound in Detecting Atelectasis in Patients Undergoing Peripheral Bronchoscopy

Study summary

This trial studies how well radial-probe endobronchial ultrasound works in detecting the complete or partial collapse of the lung in patients undergoing peripheral bronchoscopy. Diagnostic procedures, such as radial-probe endobronchial ultrasound and bronchoscopy, use a thin, tube-like instrument inserted through the nose or mouth to view and take pictures of the inside of the trachea, air passages, and lungs.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedBronchoscopy and Radial Probe Endobronchial Ultrasound

The study team can explain what participation involves.

Who it may be forMalignant Neoplasms of Respiratory and Intrathoracic Organs · Lung Neoplasm

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Nov 13, 2020 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?M.D. Anderson Cancer Center

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
M.D. Anderson Cancer Center
Interventions being studied
Procedure: Bronchoscopy; Procedure: Radial Probe Endobronchial Ultrasound
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Patients undergoing bronchoscopy with radial EBUS for peripheral lung lesions
  • Recent computed tomography (CT) performed no more than 4 weeks prior to the bronchoscopy
  • Voluntary informed consent to participate in the study
Reasons someone may not be able to joinExclusion criteria
  • Patients with baseline lung consolidation, interstitial changes or lung masses (\> 3 cm in diameter) in dependent areas of the lung as seen on most recent CT
  • Pregnancy
  • Ascites
  • Known diaphragmatic paralysis

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • M D Anderson Cancer CenterHouston, Texas

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Nov 13, 2020. Always confirm current availability with the study team.

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