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Compares treatment options for Procedural Sedation
Official title HFNO Versus Face Mask for Cerebral Oxygenation During Procedural Sedation
ClinicalTrials.gov ID: NCT07718295
What this study is testing
- What it's testing
- This prospective randomized controlled trial aims to compare the effects of high-flow nasal oxygen (HFNO) and conventional face mask oxygen therapy on cerebral oxygenation during procedural sedation performed outside the operating room. Adult patients undergoing elective diagnostic or interventional procedures under procedural sedation will be randomly assigned to receive either HFNO or conventional face mask oxygen.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Age 18 years or older
- American Society of Anesthesiologists physical status I-IV
- Scheduled for an elective diagnostic or treatment procedure performed under procedural sedation in a non-operating-room setting
- Ability to provide written informed consent
- Willingness to participate in the study
You likely can't join if
- Age younger than 18 years
- Refusal or inability to provide written informed consent
- Known neurological disorders
- History of ischemic or hemorrhagic stroke
- History of traumatic brain injury or previous cranial surgery
- Peripheral arterial disease or systemic vasculitis
See the full eligibility criteria
- Age 18 years or older
- American Society of Anesthesiologists physical status I-IV
- Scheduled for an elective diagnostic or treatment procedure performed under procedural sedation in a non-operating-room setting
- Ability to provide written informed consent
- Willingness to participate in the study
- Age younger than 18 years
- Refusal or inability to provide written informed consent
- Known neurological disorders
- History of ischemic or hemorrhagic stroke
- History of traumatic brain injury or previous cranial surgery
- Peripheral arterial disease or systemic vasculitis
- Advanced heart failure
- Uncontrolled hypertension
- Uncontrolled diabetes mellitus
- Advanced chronic obstructive pulmonary disease (COPD)
- Severe anemia (hemoglobin \<8 g/dL)
- Skin lesions or other conditions preventing proper placement of NIRS sensors
- Nasal deformity or nasal obstruction preventing the use of high-flow nasal oxygen therapy
- Any condition that, in the opinion of the investigators, could interfere with study participation or the interpretation of study results
The study team makes the final eligibility decision.
Where it's taking place
- Elâzığ, Elâzığ, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Elâzığ, Elâzığ, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.