Measurement of Endotracheal Tube Cuff

July 2, 2024 updated by: Cevdet YARDIMCI, Bozok University

Evaluation of Endotracheal Tube Cuff Pressure Measurements

The purpose of this study is to evaluate whether the endotracheal intubation practitioners accordance to the literature knowledge of cuff pressure limits.

Study Overview

Status

Active, not recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

37

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
    • Merkez/Yozgat
      • Yozgat, Merkez/Yozgat, Turkey, 66100
        • Yozgat Bozok Üniversitesi Araştırma ve Uygulama Hastanesi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

All intubated patients

Description

Inclusion Criteria:

Intubated Patients

Exclusion Criteria:

No intubation Hemodynamically unstability

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Endotracheal Intubated Group
Endotracheal tube insertion applied group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Endotracheal tube cuff pressure measurements
Time Frame: 3 months
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Bozok University

Investigators

  • Principal Investigator: Cevdet YARDIMCI, Anesthesiology and Reanimation

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 3, 2024

Primary Completion (Estimated)

September 3, 2024

Study Completion (Estimated)

October 3, 2024

Study Registration Dates

First Submitted

July 2, 2024

First Submitted That Met QC Criteria

July 2, 2024

First Posted (Actual)

July 10, 2024

Study Record Updates

Last Update Posted (Actual)

July 10, 2024

Last Update Submitted That Met QC Criteria

July 2, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2024-05-006

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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