Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
35 participants
INTERVENTIONAL
2017-03-01
2018-02-06
Brief Summary
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Detailed Description
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The hypothesis of this study is using high flow nasal oxygen therapy in the CO poisoning may be more effective and safer treatment method comparing to standard oxygen therapy in the ED. Also, it may be a safe promising alternative of hyperbaric oxygen therapy.
The aim of the study is to determine the half-life of COHb in CO-poisoned patients with high flow nasal oxygen therapy in the ED.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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HFNC therapy
Fisher\&Paykel AIRVO™ 2 High Flow Nasal Cannula Therapy will be implemented to CO-poisoned patients. Oxygen flow rate will be started 60 L/min and be decreased as the patient has requested.
Fisher&Paykel AIRVO™ 2 High Flow Nasal Cannula Therapy
A high flow nasal cannula will be implemented to the CO-poisoned patients. In the meantime, intravenous access and cardiac monitorization will have been establishing. When the high flow nasal cannula becomes ready, the first venous blood sample will be taken and the treatment will be started without any delay. The gas flow rate will be started at the rate of 30 liters per minute and will be increased to the max flow rate which patient can tolerate and FiO2 of 1.0. If the first COHb level is lesser than 10%, the patient will be excluded and will receive standard emergency care.
The blood sample will be drawn from existing IV access every 10 minutes until the COHb levels become %50 or lesser of the initial level.
Once the COHb level becomes 50% of initial measurement, following blood samples will be taken in every 30 minutes.
Interventions
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Fisher&Paykel AIRVO™ 2 High Flow Nasal Cannula Therapy
A high flow nasal cannula will be implemented to the CO-poisoned patients. In the meantime, intravenous access and cardiac monitorization will have been establishing. When the high flow nasal cannula becomes ready, the first venous blood sample will be taken and the treatment will be started without any delay. The gas flow rate will be started at the rate of 30 liters per minute and will be increased to the max flow rate which patient can tolerate and FiO2 of 1.0. If the first COHb level is lesser than 10%, the patient will be excluded and will receive standard emergency care.
The blood sample will be drawn from existing IV access every 10 minutes until the COHb levels become %50 or lesser of the initial level.
Once the COHb level becomes 50% of initial measurement, following blood samples will be taken in every 30 minutes.
Eligibility Criteria
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Inclusion Criteria
* The patients who accept to participate in the study.
Exclusion Criteria
* The patients who need mechanical ventilation
* The patients who are implemented oxygen more than 30 minutes before the ED admission
* The patients who will be transferred to the hyperbaric oxygen center before the CoHB levels are decreased to the half.
18 Years
ALL
No
Sponsors
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Kocaeli University
OTHER
Responsible Party
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Ibrahim Ulas Ozturan
Principle Investigator, MD
Principal Investigators
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Elif Yaka, Assoc. Prof.
Role: STUDY_CHAIR
Kocaeli University
İbrahim U Özturan
Role: PRINCIPAL_INVESTIGATOR
Kocaeli University
Locations
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Kocaeli University Medical Faculty
Kocaeli, Izmit, Turkey (Türkiye)
Countries
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Other Identifiers
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KIA 2016/286
Identifier Type: -
Identifier Source: org_study_id
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