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High Flow Nasal Cannula in Patients Undergoing Colonoscopy

High-flow Nasal Cannula Oxygen Therapy for Outpatients Undergoing Colonoscopy: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05687045
Enrollment
36
Registered
2023-01-17
Start date
2023-02-01
Completion date
2023-06-30
Last updated
2023-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colonoscopy

Keywords

colonoscopy, High Flow Nasal Cannula, Gas exchange

Brief summary

During colonoscopy, the insertion of the fiberscope and colon distension required to perform the examination may induce modifications to respiratory mechanics, respiratory effort and breathing pattern. High-flow nasal cannula (HFNC) therapy is a mixed air-oxygen supply system able to deliver heated humidified gas up to 60 L/min of flow rate, with an inspiratory oxygen fraction (FiO2) ranging from 21% to 100%. Increasing evidence supports the use of HFNC in several clinical conditions and settings. When compared to standard therapy (ST), HFNC results in enhanced gas exchange and improved comfort. No studies have yet assessed the benefits of HFNC versus ST during and after colonoscopy. The investigators designed this unblinded randomized controlled trial to assess whether HFNC, compared to ST, improves oxygenation at the end of the procedure (primary endpoint). Additional endpoints were: 1) the lowest peripheral saturation of oxygen (SpO2) and the number of oxygen desaturations; 2) the changes of end-expiratory lung impedance and tidal impedance assessed by Electrical Impedance Tomography (EIT); 3) the effects on diaphragm function assessed by ultrasound (DUS).

Interventions

DEVICEHigh Flow Nasal Cannula

High Flow Nasal Cannula will be set at 60 liters per minute of air/oxygen admixture to reach a peripheral oxygen saturation equal or greater than 94%

Conventional Oxygen Therapy will be administered through nasal cannula with a oxygen flow set to achieve a peripheral oxygen saturation equal or greater than 94%

Sponsors

University Magna Graecia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* outpatients with the indication to diagnostic colonoscopy

Exclusion criteria

* life-threatening cardiac aritmia or acute miocardical infarction within 6 weeks * need for invasive or non invasive ventilation * presence of pneumothorax or pulmonary enphisema or bullae * recent (within 1 week) thoracic surgery * presence of chest burns * presence of tracheostomy * pregnancy * nasal or nasopharyngeal diseases * dementia * lack of consent or its withdrawal

Design outcomes

Primary

MeasureTime frameDescription
Arterial blood gases at end of the procedureAt the end of the endoscopyArterial blood will be sample for gas analysis

Secondary

MeasureTime frameDescription
Respiratory effort at baselineAt enrollmentThe respiratory effort will be assessed through the ultrasonographic assessment of the diaphragm thickening fraction
Respiratory effort at the beginning of the colonoscopyAt 5 minutes after the beginning of the procedureThe respiratory effort will be assessed through the ultrasonographic assessment of the diaphragm thickening fraction
Respiratory effort after the colonoscopyAfter 10 minute from the end of the endoscopyThe respiratory effort will be assessed through the ultrasonographic assessment of the diaphragm thickening fraction
Respiratory effort at end of the procedureAt the end of the endoscopyThe respiratory effort will be assessed through the ultrasonographic assessment of the diaphragm thickening fraction
Change of end-expiratory lung impedance (dEELI) from baseline at end of the procedureAt the end of the endoscopy, compared to baselinechange from baseline, expressed in mL, of the end expiratory lung volume as assessed through electrical impedance tomography
Change of end-expiratory lung impedance (dEELI) from baseline after colonoscopyAfter 10 minute from the end of the endoscopy, compared to baselinechange from baseline, expressed in mL, of the end expiratory lung volume as assessed through electrical impedance tomography
Arterial blood gases at baselineAt enrollmentArterial blood will be sample for gas analysis
Change of end-expiratory lung impedance (dEELI) from baseline at the beginning of the colonoscopyAt 5 minutes after the beginning of the procedurechange from baseline, expressed in mL, of the end expiratory lung volume as assessed through electrical impedance tomography

Countries

Italy

Contacts

Primary ContactFederico Longhini, MD
longhini.federico@gmail.com+393475395967

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026