Obesity, Morbid Clinical Trial
— EPO2-AOfficial title:
EPO2-A: Evaluation of Different Pre-Oxygenation Condition in Morbid Obesity: Effect of Position and Positive Pressure Ventilation During General Anesthesia Induction
NCT number | NCT02590406 |
Other study ID # | IUCPQ 21211 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2015 |
Est. completion date | March 2016 |
Verified date | March 2020 |
Source | Laval University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The risk of complication associated with airway in obese patient is important. The result of pre-oxygenation gives the clinician a prolonged non-hypoxic apnea time. The relation between FRC and non-hypoxic apnea time has been correlated. However, the best condition to accomplish the pre-oxygenation in morbidly obese patient has yet to be described in the medical literature. A study previously done in our hospital (EPO2-PV) compared the effect of different positions and ventilation modes on the FRC in the laboratory. A significant difference has been established on the FRC between the inverse Trendelenburg position with positive pressure ventilation and the head up ("beach-chair") position without positive pressure. The current study, EPO2-A is designed to compared the two positions and ventilation modes during the induction of general anesthesia on morbidly obese and correlate the difference in FRC to difference in apnea time.
Status | Completed |
Enrollment | 50 |
Est. completion date | March 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years to 70 Years |
Eligibility |
Inclusion Criteria: - BMI > 40 - Abdominal obesity : waist circumference: > 115 for the women waist circumference > 130 for the men Exclusion Criteria: - Facial hair - Cranio-facial abnormality - Asthma (continuous treatment) - COPD (FEV1 < 80%) - Severe cardiovascular disease (NYHA > 3) - Pregnancy - Tobacco use - Know or suspected difficulty with intubation - Severe GERD or risk of aspiration |
Country | Name | City | State |
---|---|---|---|
Canada | Institut universitaire de cardiologie et de pneumologie de Québec | Québec city | Quebec |
Lead Sponsor | Collaborator |
---|---|
Laval University |
Canada,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Non Hypoxic Apnea Time | Change of Non-hypoxic apnea time in obese patient during a General Anesthesia induction, as a result of different pre-oxygenation position and ventilation mode; 1-Beach Chair and No positive pressure ventilation, 2-Reverse Trendelenburg and positive pressure ventilation and PEEP. End of measure time frame is 5 minutes after intubation | After a 3 minutes pre-oxygenation period | |
Secondary | Time to Expired Oxygen Fraction > 0,9 | Evaluation of time needed to obtain an expired fraction of oxygen of > 0,9 in the two groups during the pre-oxygenation | During the pre-oxygenation period | |
Secondary | Maximum Expired Fraction of Oxygen Obtained | Evaluation of the maximum expired oxygen fraction obtained in the two groups | After 3 minutes of pre-oxygenation | |
Secondary | Minimum Arterial Saturation of Oxygen Obtained | Evaluation of the minimal saturation obtained after the resumption of the ventilation | After the end of the Non-hypoxic apnea time | |
Secondary | Time to 97% Saturation | Evaluation of the time needed to the beginning of the ventilation to the moment where the saturation is 97% | ||
Secondary | Hemodynamic Changes | Evaluation of the changes in vital signs during and after the pre-oxygenation phase in the two combinations of position and ventilation mode | From the beginning of the pre-oxygenation to the end of the protocol |
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