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Nasopharyngeal Airway Facilitate Transnasal Humidified Rapid Insufflation Ventilatory Exchange

Nasopharyngeal Airway Facilitate Transnasal Humidified Rapid Insufflation Ventilatory Exchange

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03741998
Enrollment
120
Registered
2018-11-15
Start date
2018-11-07
Completion date
2019-12-30
Last updated
2019-07-22

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

Conditions

Hypercapnia, Hypoxia

Brief summary

For performing transnasal humidified rapid insufflation ventilatory exchange (THRIVE), jaw-thrust maneuver have to maintain to make sure the airway open and the CO2 clearance during apnoea. The objective of present study is to prove that nasopharyngeal airway facilitate THRIVE and no need jaw-thrust maneuver and maintain the similar PO2 and PCO2 during apnoea.

Interventions

THRIVE with a regular nasopharyngeal airway.

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Signed informed consent. * Undergoing surgery with general anaesthesia. * Adult, \>18 years old. * American Society of Anesthesiology classification I-II.

Exclusion criteria

* Coagulation disorders or a tendency of nose bleeding * An episode/exacerbation of congestive heart failure (CHF) that requires a change in medication, diet or hospitalization from any cause in the last 6 months * Severe aortic stenosis or mitral stenosis; * Cardiac surgery involving thoracotomy (e.g., coronary artery bypass graft (CABG), valve replacement surgery) in the last 6 months; * Acute myocardial infarction in the last 6 months; * Acute arrhythmia (including both tachycardia and bradycardia) with hemodynamic instability; * Diagnosed COPD or current other acute or chronic lung disease requiring supplemental chronic or intermittent oxygen therapy); * Increased intracranial pressure; * ASA \>II; * Mouth, nose, or throat infection; * Fever, defined as core body temperature \> 37.5°C; * Pregnancy, breastfeeding or positive pregnancy test; * Emergency procedure. * Patient with known or suspected difficult airway

Design outcomes

Primary

MeasureTime frame
The partial pressure of carbon dioxide (pCO2)From start to end of THRIVE(20 minutes)
The partial pressure of oxygen(PO2)From start to end of THRIVE(20 minutes)

Countries

China

Contacts

Primary ContactDiansan Su, Dr.
diansansu@yahoo.com+862168383702

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026