Transition to Ambulatory Bariatric Surgery (TABS) Trial
Recruiting
N/A
Interventional Study
Obesity and Obesity-related Medical Conditions
Bariatric Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 25 – 55
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 200 (estimated)
- Sponsor
- Vanderbilt University Medical Center · Other
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About This Trial
This study will compare same day discharge and at least one night stay in the hospital after bariatric surgery. Patients undergoing bariatric surgery will be randomized (i.e. have an equal chance of either plan) to either group. The study's primary outcome is the frequency patients in the study require a visit to the emergency room within 7 days of their surgery.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* BMI ≤ 60 kg/m2
* Primary Sleeve gastrectomy or Gastric Bypass,
* Undergoing bariatric surgery at sponsor site
Exclusion Criteria:
* Type 1 Diabetes
* Myocardial Infarction
* Unstable Angina or Heart Failure
* Prior Stroke
* Solid organ transplantation
* Systemic glucocortico…
Contacts