Clinical Trial: Accelerated Recovery Protocol in Patients Undergoing Bariatric Surgery
- Conditions
- unspecified obesity
- Registration Number
- RBR-7hfd5rc
- Lead Sponsor
- Casa de Saúde Santa Marcelina
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients aged between 18 and 60 years; able to read, understand and sign the consent form; undergoing the first procedure for the treatment of obesity
patients with a BMI above 60 kg/m2; patients with chronic pain with continuous use of medications for pain control, such as fibromyalgia and non-eventual low back pain; patients with heart and coronary diseases; ventricular ejection fraction less than 50%; anticoagulation with warfarin; patients with chronic kidney disease on dialysis; patients with mobility and ambulation difficulties; prolonged surgical time (greater than 3 hours) or need for conversion to open surgery; patients referred to the intensive care unit (ICU) after the procedure; need for drainage of the abdominal cavity; latex allergy; allergy to any of the medications used in the protocol
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected Outcome: Impact of the intervention on the length of stay, assessed through data from the medical record, with an expected decrease of 25% in the length of stay in the hospital, measured in hours.
- Secondary Outcome Measures
Name Time Method