New monitoring method tested for brain death diagnosis
NCT ID NCT06983990
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This completed study looked at 35 patients undergoing apnea testing for brain death. Researchers checked if non-invasive oxygen and carbon dioxide monitors could give the same information as standard blood tests. The goal was to see if these simpler methods could be used instead of repeated blood draws.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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35 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Jun 2025
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study will include adult patients (aged 18 and over) who are being monitored in the intensive care units of the University of Health Sciences Bursa Yuksek Ihtisas Training and Research Hospital and are suspected of brain death, for whom an apnea test has been scheduled by their physician as part of the brain death diagnosis process. The study population will consist of patients who meet the inclusion criteria and for whom written informed consent has been obtained from a legally authorized representative. Patients whose first-degree relatives have declined participation, and those in whom the Oxygen Reserve Index (ORI) probe cannot be used due to circulatory disorders in the extremities, will be excluded from the study.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients who meet all the prerequisites for initiating the brain death diagnosis process and for whom the decision to perform the apnea test for diagnosis of brain death. * Patients aged 18 years or older. * Patients who have provided verbal and written consent from their first-degree relatives. Exclusion Criteria: * Patients whose first-degree relatives do not consent to participation in the study. * Patients in whom the ORI probe cannot be used due to circulatory disturbances in the extremities
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Health Sciences University Bursa Yüksek İhtisas Training and Research Hospital
Bursa, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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