Morbid Obesity Clinical Trial
Official title:
Application of Protective Ventilation Improves Oxygenation During and After Anesthesia. Is it Possible That a Special Procedure, an Oxygenation Test, Can Replace Arterial Blood Gases When Evaluating Oxygenation?
Verified date | August 2014 |
Source | Landstinget Västmanland |
Contact | n/a |
Is FDA regulated | No |
Health authority | Sweden: Regional Ethical Review Board |
Study type | Interventional |
The study investigates if applying a special ventilatory strategy during anesthesia for
laparoscopic gastric by pass, produces less atelectasis and better oxygenation in spite of
using 100 % oxygen during pre oxygenation and induction of anesthesia. The study
investigates oxygenation with blood gas samples but also with a new method that might give
more information without the use of blood gas samples.
Primary: Oxygenation in patients with morbid obesity improves if preoxygenation, induction
and maintenance of anesthesia is performed with either a continuous positive airway pressure
(CPAP) or a positive end expiratory pressure (PEEP), respectively, of 10 cm H2O, in
comparison to a technique without CPAP but with a PEEP of 10 cm H2O.
Secondary: The improved oxygenation during anesthesia can be prolonged inte the
postoperative period if emergence from anesthesia is performed without high levels of
oxygen.
Status | Completed |
Enrollment | 40 |
Est. completion date | March 2014 |
Est. primary completion date | March 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Adult patients scheduled for elective surgery of Morbid Obesity. - ASA 1-2. (ASA = American Society of Anesthesiologists classification). - "Body mass index" (BMI) = 35 but < 50 Exclusion Criteria: - "ASA 3" - Anticipated difficult intubation. - Major bleeding. - Problems with ventilation necessitating protocol aberrations. - Obstructive sleep apnea syndrome with CPAP treatment at home. - Angina Pectoris |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Sweden | Operationskliniken, Västmanlands sjukhus Västerås | Västerås |
Lead Sponsor | Collaborator |
---|---|
Landstinget Västmanland |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in peripheral O2 saturation(SpO2)during and 1 hour after anesthesia in comparison to awake before anesthesia. | During anesthesia SpO2 is measured at three different levels of oxygen; 21, 26 and 31 % respectively as long as SpO2 does not go lower than 87 % and compared to SpO2 immediately before anesthesia. SpO2 breathing air one hour after anesthesia is compared to SpO2 before anesthesia. | Change in SpO2 from 5 min before start of anesthesia, to 5 min after intubation, 5 min before extubation and 1 hour after extubation. | Yes |
Secondary | Arterial blood gas values for saturation (SaO2) | During anesthesia SaO2 is measured at three different levels of oxygen; 21, 26 and 31 % respectively as long as SpO2 (sic! does not go lower than 87 % and compared to SaO2 immediately before anesthesia. SaO2 breathing air one hour after anesthesia is compared to SaO2 before anesthesia. | 5 min before anesthesia, 5 min after intubation, 5 min before extubation and 1 hour after anesthesia. | Yes |
Secondary | Arterial oxygen tension (PaO2) | During anesthesia PaO2 is measured at three different levels of oxygen; 21, 26 and 31 % respectively as long as SpO2 (sic) does not go lower than 87 % and compared to PaO2 immediately before anesthesia. PaO2 breathing air one hour after anesthesia is compared to PaO2 before anesthesia. | 5 min before start of anesthesia, 5 min after intubation, 5 min before extubation and 1 hour after extubation. | Yes |
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