THRIVE Use in Pediatric Populations- Multi Site
- Conditions
- HypoventilationAnesthesia; Adverse EffectDesaturation of BloodOxygen Deficiency
- Interventions
- Device: Transnasal Humidified Rapid-Insufflation Ventilatory Echange
- Registration Number
- NCT04322994
- Lead Sponsor
- Stanford University
- Brief Summary
THRIVE (Transnasal Humidified Rapid-Insufflation Ventilatory Exchange) refers to the use of high-flow nasal cannula to augment the ability to oxygenate and ventilate a patient under general anesthesia. The use of high-flow nasal cannula oxygen supplementation during anesthesia for surgical procedures has been a recent development in the adult population, with limited data analyzing the pediatric population. This study will determine whether high flow nasal cannula oxygen supplementation during surgical or endoscopic procedures can prevent desaturation events in children under anesthesia and improve the outcomes of that surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 500
- Pediatric patients less than 18 years of age undergoing general anesthesia for procedures or surgeries
- Pregnancy
- Absence of parent or legal guardian able to provide written consent for study participation
- Anatomical or surgical contraindications (epistaxis, basilar skull fractures or abnormalities, nasal surgery or obstruction, nasal fractures, nasal vascular abnormalities), tracheostomy tube
- Emergent surgery for which application of HFNC might delay surgery or might result in increased aspiration risk.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Transnasal Humidified Rapid-Insufflation Ventilatory Echange Treatment subjects will undergo the scheduled procedure, with the difference being that a high-flow nasal cannula will be applied prior to the start of the procedure and removed following the procedure's conclusion. While applied, the cannula will deliver high- flow rate oxygen, air, or a mixture of variable oxygen concentration (21-100%) depending on the surgical conditions and requirements. The rate will be set at 1-4L/kg/min with a maximum of 70L/min. Participants in the treatment arm will then proceed to the recovery area as usual. Following recovery from anesthesia, a brief questionnaire will be provided to applicable patients or their parents / guardians / representatives. Intervention: Device: High-flow nasal cannula
- Primary Outcome Measures
Name Time Method Group differences in oxygen desaturation index Duration of surgery or procedure by second, which is generally less than 2 hours Oxygen desaturation index is defined as a 4% decrease in saturation from a 120 second rolling mean for greater than 10 seconds
Incidence of oxygen desaturation Duration of surgery or procedure by second, which is generally less than 2 hours Absolute incidence of oxygen desaturation less than 90% as measured by pulse oximetry by second
Relative incidence of desaturations <90% or defined by a 5% fall from baseline if baseline saturation < 94%. Duration of surgery or procedure, which is generally less than 2 hours Relative incidence of oxygen desaturation less than 90% as measured by pulse oximetry by second adjusted for post surgical diagnosis
- Secondary Outcome Measures
Name Time Method Duration and severity of desaturations <90% Duration of surgery or procedure by second Duration and severity of oxygen desaturation less than 90% as measured by pulse oximetry by second by analyzing area under curve less than 90%
Relative number of surgical interruptions due to desaturation Duration of surgery or procedure Number of surgical interruptions due to desaturation defined by a pause in surgical procedures due to need to intervene to improve patient's oxygen saturation, normalized to case length
Relative number and severity of airway interventions due to desaturation Duration of surgery or procedure by second, which is generally less than 2 hours Number of Jaw thrust, bag mask ventilation, and/or endotracheal intubations due to desaturation, normalized by case length
Trial Locations
- Locations (5)
Lucile Packard Children's Hospital Stanford
🇺🇸Palo Alto, California, United States
The University of Virginia
🇺🇸Charlottesville, Virginia, United States
Lurie Children's Hospital of Chicago
🇺🇸Chicago, Illinois, United States
Massachussetts Eye and Ear Harvard Medical School
🇺🇸Boston, Massachusetts, United States
Cincinnati Children's Hospital
🇺🇸Cincinnati, Ohio, United States