Implementation of Apnoea Test for Patients With Suspected Brain Death

Implementation of Apnoea Test for Patients With Suspected Brain Death (IMAPing SUBDEP)

This study consists of a survey created for intensive care physicians regarding their current practice of the implementation of apnoea test for patients with suspected brain death.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Although the apnoea test is part of nearly all protocols for determining brain death; implementation significantly differs among intensive care physicians according to national-level acts, national society protocols or local protocols.

This cross-sectional study is based on an international, web-based questionnaire created for intensive care physicians, consisting of 25 questions in English.

The survey will provide a current state of the practice of apnoea testing in patients with suspected brain death. The results can support the determination of future acts to standardize the apnoea test process.

The given answers are anonymous. The e-mail address of the respondent is not recorded. Answers are treated solely for scientific purposes.

Study Type

Observational

Enrollment (Estimated)

200

Contacts and Locations

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

Study Contact

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Any physician working in intensive care can fill the form and participate in the study.

Description

Inclusion Criteria:

  • Physicians working in intensive care units

Exclusion Criteria:

-

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of apnoea tests
Time Frame: last 1 year
How much apnoea test is required for brain death determination.
last 1 year
Timeframe between apnoea tests
Time Frame: last 1 year
If more than 1 apnoeae test is reuired for brain death determination, how many hours should elapse between the two tests.
last 1 year
Preoxygenation
Time Frame: last 1 year
For how long (in minutes) the patient is preoxygenated before the apnoea test.
last 1 year
Baseline arterial carbon dioxide (CO2) level
Time Frame: Last 1 year
What is the required arterial partial CO2 pressure (PaCO2) before apnoea testing, confirmed by arterial blood gas measurement?
Last 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Detection of possible spontaneous breath movements
Time Frame: last 1 year
To determine if any observation method other than visualisation by the observer is used to determine possible spontaneous breath movements during the apnoea test.
last 1 year
Satisfaction with current practice
Time Frame: last 1 year
Surveying the satisfaction of physicians with current practice regarding the method of the detection of spontaneous breath movements on a 4 grade scale (1 - non-reliable to 4 - very reliable).
last 1 year

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Continuous positive airway pressure (CPAP)
Time Frame: last 1 year
If a CPAP system is used during apnoea test, what is the value of positive end-expiratory pressure (PEEP) in H2Ocm.
last 1 year

Collaborators and Investigators

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

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 (Estimated)

May 1, 2024

Primary Completion (Estimated)

July 31, 2024

Study Completion (Estimated)

July 31, 2024

Study Registration Dates

First Submitted

March 27, 2024

First Submitted That Met QC Criteria

April 8, 2024

First Posted (Actual)

April 11, 2024

Study Record Updates

Last Update Posted (Actual)

May 6, 2024

Last Update Submitted That Met QC Criteria

May 3, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

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.

Clinical Trials on Brain Death

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