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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02968706
Other study ID # 2016-516
Secondary ID
Status Recruiting
Phase N/A
First received November 8, 2016
Last updated February 17, 2017
Start date January 2017
Est. completion date October 2017

Study information

Verified date February 2017
Source Aventura Hospital and Medical Center
Contact Hilda Mahmoudi, MD, MPH
Phone (305) 682 7261
Email Hilda.Mahmoudi@hcahealthcare.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if high flow nasal cannula (HFNC), as compared to conventional nasal cannula, improves oxygenation and prevents desaturation events in obese patients undergoing colonoscopy.


Description:

Intravenous sedation during colonoscopy has become the standard practice in United States given its higher patient satisfaction and procedural quality. The most common used short acting sedative agent is propofol. Although possessing safe and rapidly reversed pharmacokinetic properties, propofol intravenous infusion can lead to respiratory depression and hypoxemia. In one prospective study, hypoxemia events, defined by oxygen saturation less than 90 percent was found in 20 percent of patients receiving colonoscopy using propofol sedation. The mechanism of hypoxemia is mainly hypoventilation, airway collapse, and carbon dioxide (CO2) retention. When it comes to gastrointestinal procedures, using oxygen devices for augmenting ventilation is usually avoided, ex: positive pressure ventilation, since it can lead to bowel distention and affect quality of procedures. Therefore most hospitals in United States still use nasal cannula of oxygen therapy during gastrointestinal procedures, and there is lack of available options of oxygen therapy which can improve hypoventilation and prevent hypoxemia.

High flow nasal cannula (HFNC) is a new generation of oxygen therapy. It provides constant high flow oxygen delivery with heated and humidified air. Moreover, it has been studied that high velocity of airflow can create the effect of "positive end expiratory pressure" thus assist ventilation and work of breathing. Compared to conventional nasal cannula and face mask, HFNC has demonstrated superior performance in oxygenation, work of breathing and patient comfort in many studies. Since its invention, HFNC has been studied in post-cardiac surgery, post-extubation, bronchoscopy and dental procedures and all of them show equal to better oxygen performance in comparison of nasal cannula.

While capnographic monitoring has been studied to prevent hypoxemia during sedation, no studies have been done to evaluate the clinical utility of new generation oxygen therapy. Obesity is associated with increased frequency of sedation related complications especially hypoxemia during propofol mediated sedation for advanced endoscopic procedures. The Investigators hypothesized that HFNC may improve oxygen performance compared to conventional nasal cannula for obese patients receiving colonoscopy under intravenous sedation.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date October 2017
Est. primary completion date October 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- BMI = 30.

- Age = 18 years.

- ASA classification II and III.

- Scheduled for colonoscopy.

- Able to provide written informed consent.

Exclusion Criteria:

- Allergic to propofol and any of its contents.

- Baseline SpO2 less than 93%.

- Patients who require intubation for airway protection based on anesthesiologist discretion.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
High Flow Nasal Cannula
Heated humidified high flow oxygen of 50 L/min at FiO2 of 40%
Conventional Nasal Cannula
Supplemental oxygen of 2-5 L/min
Other:
Patient satisfaction questionnaire
Questionnaire

Locations

Country Name City State
United States Aventura Hospital and Medical Center Aventura Florida

Sponsors (1)

Lead Sponsor Collaborator
Aventura Hospital and Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence rate of desaturation events during procedures (desaturation events are defined by either SpO2 drops more than 5% compared to baseline SpO2 OR SpO2<90% at any time of procedures) Through out the colonoscopy procedure (after propofol induction to the end of colonoscopy)
Secondary Incidence rate of carbon dioxide retention (end tidal CO2 more than 50 mmHg at any time of procedure) Through out the colonoscopy procedure (after propofol induction to the end of colonoscopy)
Secondary Patients satisfaction level (patient comfort and mouth dryness assessed by a questionnaire with 4-scale questions) One time point (15 minutes after the patient recovered from anesthesia sedation)
Secondary Respiratory rates before and after colonoscopy procedure, and highest respiratory rate during colonoscopy procedure. Three time points (Before, through out, and within 5 minutes after the colonoscopy procedure)
Secondary Incidence rate of hypoxia rescue intervention events (e.g. jaw lift, anterior mandibular shifting, head elevation ) Through out the colonoscopy procedure
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