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Continuous Endotracheal Cuff Pressure Control to Prevent Ventilator Associated Respiratory Infections

NCT02966392 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2020-05-29

No results posted yet for this study

Summary

The purpose of the study is to determine whether automated cuff pressure control results in a reduction in the proportion of patients developing ventilator associated respiratory infections during their stay in intensive care.

Conditions

  • Mechanical Ventilation Complication
  • Tracheal Intubation Morbidity
  • Ventilator-Associated Pneumonia
  • Hospital Acquired Infection

Interventions

DEVICE

Tracoe cuff pressure controller

Participant will be attached to the cuff pressure controller as soon as possible after enrolment. They will remain attached during their intubated stay. If reintubated during same admission they will continue in the intervention arm. If readmitted to ICU they will be managed according to standard care.

Sponsors & Collaborators

  • The Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam

    collaborator UNKNOWN

  • Trung Vuong Hospital, Ho Chi Minh City, Vietnam

    collaborator UNKNOWN

  • The National Hospital for Tropical Diseases, Ha Noi, Vietnam

    collaborator UNKNOWN

  • Oxford University Clinical Research Unit, Vietnam

    lead OTHER

Principal Investigators

  • Behzad Nadjm, MBChB MD · Oxford University Clinical Research Unit

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-01
Primary Completion
2019-03-07
Completion
2019-09-30

Countries

  • Vietnam

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 NCT02966392 on ClinicalTrials.gov