Electric Blower Based Ventilator Used During Procedural Sedation

Utah System of Higher Education (USHE)

Status: Completed

Conditions: Apnea During Procedural Sedation

Treatments: Device: Noninvasive Ventilator (V60, Philips)

Study type: Interventional

Funder types: Other; Other U.S. Federal agency

Identifiers

NCT02621463

IRB_00074281

Details and patient eligibility

About

Conduct human trials in the endoscopy suite of our continuous positive airway pressure (CPAP) ventilator approach using an FDA approved ventilator.

Full description

All study procedures will be performed in adult patients following informed consent at the endoscopy suite of the University of Utah Health Sciences Center in Salt Lake City, Utah. A ventilation mask will be placed on the patient's face and connected to the ventilator. Supplemental oxygen will be delivered by the ventilator through the mask; the concentration of oxygen delivered will be left to the clinician's discretion. A modified mask with multiple small leaks will be used with a standard elastomeric H-strap to secure it to the patient's face.

The endoscopy suite nurse and technicians will attach all clinically necessary standard sensors and connect them to the patient and monitoring system. Height, weight, and neck circumference will be measured and recorded digitally on an encrypted laptop. In addition to the standard of care monitors, the investigators will collect data from additional non-invasive modalities and save the data to a laptop using custom software for later analysis.

Pressure and flow sensors included in the ventilator will be used to monitor the patients' tidal volumes and respiratory rate during the procedure. The data that will be collected and recorded on the laptop will include: RIP data, mask pressure, flow, and breath rate. An additional flow sensor will be placed in line with the ventilator.

The objective of this study is threefold: Demonstrate in patients undergoing procedural sedation (e.g., for colonoscopy) that obstructive apnea can successfully be avoided by stenting the airway open using CPAP, demonstrate that we can successfully detect periods of zero ventilation, and demonstrate the functionality of the modified standard mask.

Enrollment: 29 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• > 18 years of age
• undergoing a colonoscopy procedure
• receiving registered nurse-administered procedural sedation at the University of Utah Health Sciences Center
• agree to participate
• written informed consent

Exclusion criteria

• Inability/refusal of subject to provide informed consent.
• Standard colonoscopy exclusion criteria used at the GI lab at the University of Utah.
• Pregnant patients and patients with an ASA (American Society of Anesthesiology) physical status of IV or V.
• Patients with severe medical condition(s) that in the view of the acting physician prohibits participation in the study.
• Patients with a BMI > 35 will not be included in the study

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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29 participants in 1 patient group

Noninvasive Ventilation

Experimental group

Description:

Use of the Noninvasive Ventilator (V60, Philips). The ventilator mask will be placed on the patient's face according to their comfort using an elastomeric H-strap. CPAP of 8 cmH2O (pressure) will be the starting setting for the ventilator.

Treatment:

Device: Noninvasive Ventilator (V60, Philips)