Morbid Obesity Clinical Trial
— EPO2-PVOfficial title:
Evaluation of Different Pre-Oxygenation Conditions in Morbid Obesity: Position and Ventilation Mode, in a Respiratory Physiology Laboratory, on Voluntary Subjects
Verified date | September 2017 |
Source | Laval University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The risk of complications associated with airway management in obese patients is significant.
The results of pre-oxygenation allow a prolonged non-hypoxic apnea time for the clinician.
The increase in FRC and non-hypoxic apnea time is correlated. The best condition to
accomplish the pre-oxygenation in morbidly obese patient is still undetermined in medical
literature.
This study is designed to evaluate the effect of different positions combined with different
ventilation modes during the pre-oxygenation phase of anesthesia's induction. EPO2: PV will
evaluate the effect of different combinations of positions and ventilation modes on pulmonary
volumes (mainly functional residual capacity) in a morbidly obese volunteer.
Status | Completed |
Enrollment | 20 |
Est. completion date | July 2014 |
Est. primary completion date | June 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - BMI 40 - 80 kg / m2 - Waist circumference: Men: More than 130 cm - Waist circumference: Women: More than 115 cm Exclusion Criteria: - Facial hair - Cranio-facial abnormality - Claustrophobia - Asthma - COPD (defined by FEV1 < 80 %) - Severe cardiovascular disease (defined by NYHA =3) - Pregnancy - Tobacco use - NI-CPPV Intolerance documented by a respiratory specialist (pneumologist). |
Country | Name | City | State |
---|---|---|---|
Canada | Institut universitaire de cardiologie et de pneumologie de Québec | Quebec city | Quebec |
Lead Sponsor | Collaborator |
---|---|
Laval University |
Canada,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Vital Signs | Change in vital signs before and after the pre-oxygenation phase in the 6 combinations after a 5 minutes pre-oxygenation period in the 6 combinations previously described. | At the end of a 5 minutes pre-oxygenation period | |
Primary | Functional Residual Capacity | Change of functional residual capacity (FRC), in obese patient, as a result of different pre-oxygenation positions; 1- supine, 2-beach-chair, 3- reverse Trendelenburg, in two different ventilation modes : 1- spontaneous ventilation at tidal volume, 2- non-invasive positive pressure ventilation with inspiratory assistance. | After a 5 minutes pre-oxygenation period | |
Secondary | Diaphragmatic Amplitude. | Evaluation of changes in diaphragmatic amplitude and movement determined by fluoroscopy imaging after a 5 minutes pre-oxygenation period in the 6 combinations previously described. | After a 5 minutes pre-oxygenation period | |
Secondary | Respiratory Mechanics | Change in respiratory mechanics (compliance, resistance, tidal volume, positive end-expiratory pressure, maximal inspiratory pressure) evaluated at the end of a 5 minutes pre-oxygenation period in the 6 combinations previously described. | At the end of a 5 minutes pre-oxygenation period | |
Secondary | Patient's Comfort | Evaluation of the patient's comfort at the end of each intervention on an analog visual scale after a 5 minutes pre-oxygenation period in the 6 combinations previously described. | At the end of a 5 minutes pre-oxygenation period |
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