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Determining the Appropriate Setting of an Automated Secretion Removal Technology (TrachFlush)

NCT05668299 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2022-12-29

No results posted yet for this study

Summary

Using a new device, the TrachFlush, the aim of this pilot study is to investigate whether secretions can be removed at the patient's current ventilator settings, or whether pressures and durations considered at the maximal end of clinical practice are required, so as to push secretions around the cuff. The study is a pilot study to investigate the settings required to ensure clinical efficacy of the technology, prior to large scale clinical studies.

Conditions

  • Mechanical Ventilation Complication
  • Intubation Complication

Interventions

DEVICE

TrachFlush

See detailed description previously entered.

Sponsors & Collaborators

  • Viborg Regional Hospital

    collaborator OTHER

  • Herning Hospital

    collaborator OTHER

  • Aalborg University

    collaborator OTHER

  • Hospitalsenheden Vest

    lead OTHER

Principal Investigators

  • Nilanjan Dey, MD · Gødstrup Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-01
Primary Completion
2022-02-08
Completion
2022-02-10

Countries

  • Denmark

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 NCT05668299 on ClinicalTrials.gov