About this trial
The ultimate goal of this research is to optimize care for patients undergoing laparoscopic bariatric surgery while alleviating pressure on hospital resources and staff. Furthermore, the study aims to generate policy-relevant data that can inform policymakers and healthcare providers in developing funding models and care pathways that balance safety, efficiency, and cost-effectiveness. This could support a broader implementation of ambulatory bariatric surgery without compromising quality of care.
Eligibility criteria
Qualifiers
18-65 years old
Undergoing scheduled ambulatory Roux en Y Gastric Bypass
ASA score I or II
Competent to provide informed consent
Disqualifiers
Presence of coagulation abnormalities or use of anticoagulant therapy
History of major abdominal surgeries, including laparotomy
Absence of informed consent or request not to participate in the study
Trial design
Treatments tested in this trial
- remote clinical monitoring
- Control group