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Evaluation of BAL Procedure With Ambu aScope 3 Large in Patients in an ICU Setting

NCT03581474 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2020-02-13

Study results available
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Summary

An Investigation to determine the single-use scope's ability to suction secretion from the lungs to resolve the collapse of the lung.

Conditions

  • Atelectasis
  • Bronchoscopy

Interventions

DEVICE

Bronchoscopic procedure

Single-use flexible bronchoscope aScope 3 Large

Sponsors & Collaborators

  • Ambu A/S

    lead INDUSTRY

Principal Investigators

  • Anna Charlotte Lundgaard · Ambu A/S

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-28
Primary Completion
2018-07-03
Completion
2018-07-03
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03581474 on ClinicalTrials.gov