HFNO Flow Rates and Cerebral Oxygenation During Deep Sedation for Cystoscopy
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: High-Flow Nasal Oxygen 40 L/min (HF40), High-Flow Nasal Oxygen 55 L/min (HF55), High-Flow Nasal Oxygen 70 L/min (HF70).
- Кому может быть актуально
- Состояния в реестре: Deep Sedation, High Flow Nasal Canula, Cerebral Oxygenation, PSI. Базовые параметры: от 18 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Turkey (Türkiye)
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Effect of Different Flow Rates of High-Flow Nasal Oxygen on Peripheral and Cerebral Oxygenation and Ventilation During Procedural Sedation for Cystoscopy: A Prospective Randomized Controlled Trial
Обзор
For Patients and Families This study aims to investigate how high-flow oxygen therapy affects oxygen levels, especially brain oxygenation, during cystoscopy procedures performed under sedation. The goal is to improve patient safety and comfort by ensuring better oxygen delivery during the procedure. Different oxygen flow rates will be compared, while patients' breathing, oxygen levels, and vital signs are continuously monitored throughout the procedure. All methods used in the study are consistent with routine anesthesia practices, and patient safety remains the highest priority. For Healthcare Professionals This prospective randomized controlled study evaluates the effects of different high-flow nasal oxygen (HFNO) flow rates on cerebral oxygenation, peripheral oxygenation, and ventilation parameters in patients undergoing cystoscopy under procedural sedation. The primary aim is to determine the contribution of HFNO to sedation safety and to provide clinical evidence regarding the optimal flow rate. In addition, hypoxemia incidence, airway intervention requirements, hemodynamic variables, and sedation depth are being analyzed.
Вмешательства
- Устройство High-Flow Nasal Oxygen 40 L/min (HF40)
Participants receive high-flow nasal oxygen (HFNO) therapy delivered through the OptiFlow™ system at a flow rate of 40 L/min with 100% heated and humidified oxygen during procedural sedation for cystoscopy. Sedation is achieved using midazolam, remifentanil, and propofol. - Устройство High-Flow Nasal Oxygen 55 L/min (HF55)
Participants receive HFNO therapy via the OptiFlow™ system at a flow rate of 55 L/min with 100% heated and humidified oxygen during procedural sedation for cystoscopy, together with the same standardized sedation protocol. - Устройство High-Flow Nasal Oxygen 70 L/min (HF70)
Participants receive HFNO therapy via the OptiFlow™ system at a flow rate of 70 L/min with 100% heated and humidified oxygen during procedural sedation for cystoscopy, together with the same standardized sedation protocol.
Первичные конечные точки
- Change in Regional Cerebral Oxygen Saturation (rSO₂) [Срок оценки: From baseline measurement before sedation until the end of the cystoscopy procedure (intraoperative period). Cerebral oxygen saturation (rSO₂) values are recorded continuously during procedural sedation.]
Вторичные конечные точки (10)
- Peripheral Oxygen Saturation (SpO₂) [Срок оценки: From baseline measurement before sedation until the end of the cystoscopy procedure (intraoperative period). Cerebral oxygen saturation (rSO₂) values are recorded continuously during procedural sedation.]
- Partial arterial carbon dioxide pressure (PaCO₂) [Срок оценки: At baseline before the initiation of sedation and at the end of the cystoscopy procedure. Arterial blood gas analysis (PaCO₂) and end-tidal carbon dioxide (EtCO₂) measurements will be recorded at both time points.]
- End-tidal carbon dioxide (EtCO₂) [Срок оценки: At baseline before the initiation of sedation and at the end of the cystoscopy procedure. End-tidal carbon dioxide (EtCO₂) measurements will be recorded at both time points.]
- Incidence of Hypoxemia [Срок оценки: From the initiation of procedural sedation until the end of the cystoscopy procedure. Hypoxemia episodes occurring during the intraoperative sedation period will be recorded continuously.]
- Airway Intervention Requirement [Срок оценки: From the initiation of procedural sedation until the end of the cystoscopy procedure. Any airway intervention requirement occurring during the intraoperative period will be recorded.]
- Heart Rate [Срок оценки: From baseline before sedation until the end of the cystoscopy procedure. Heart rate will be recorded continuously during the intraoperative sedation period.]
- Mean Arterial Pressure [Срок оценки: From baseline before sedation until the end of the cystoscopy procedure. Blood pressure, will be recorded continuously during the intraoperative sedation period.]
- Patient State Index (PSI) [Срок оценки: From the initiation of sedation until the end of the cystoscopy procedure.]
- Modified Observer's Assessment of Alertness/Sedation (MOAA/S) Score [Срок оценки: From the initiation of sedation until the end of the cystoscopy procedure.]
- Patient Satisfaction [Срок оценки: Assessed once at the end of the recovery period immediately after completion of the cystoscopy procedure (postoperative period, approximately 30-60 minutes after the procedure).]
Критерии участия
Критерии включения
- Age ≥18 years
- Scheduled to undergo elective cystoscopy under procedural sedation in an operating room setting
- American Society of Anesthesiologists (ASA) physical status classification I-III
- Ability to provide written informed consent
Критерии исключения
- Known neurological disorders
- History of ischemic or hemorrhagic stroke
- Peripheral artery disease
- Vasculitis
- Severe heart failure
- Uncontrolled hypertension
- Uncontrolled diabetes mellitus
- Advanced-stage chronic obstructive pulmonary disease
- Severe anemia (hemoglobin <8 g/dL)
- Skin lesions that could interfere with near-infrared spectroscopy (NIRS) measurements
- History of head trauma
- History of cranial surgery
- Nasal deformity or nasal obstruction
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Тройное слепое
- Основная цель
- Скрининг
Центры проведения
Turkey (Türkiye) · 1 центр
- Fırat University Faculty of Medicine Hospital — Elâzığ
Идентификаторы
NCT: NCT07630038 · 47669