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Transition to Ambulatory Bariatric Surgery (TABS) Trial

Study acronym: TABS
StatusRecruiting
PhaseNot applicable
Started2026-10-01
View on ClinicalTrials.gov ↗

Amendment history

2026-09-22
Recruitment opened
2026-08-17
Study Status v3
Primary completion moved earlier: 2027-12-01 → 2027-10-01
Start date2026-07-01→2026-10-01
2026-05-17
Study Status v2
Start date2026-03-01→2026-07-01
2025-06-09
Study Status, Study Description, Outcome Measures, Eligibility v1
Eligibility criteria-151 characters
[...] going bariatric surgery at sponsor site Exclusion Criteria: A. Pre-Existing Condition: 1. Type 1 Diabetes, 2. Myocardial Infarction, 3. Unstable Angina or Heart Failure, 4. Prior Stroke, 5. Solid organ transplantation, 6. Systemic glucocorticoid prior 28 days, 7. Severe Obstructive Sleep Apnea, 8. Uncontrolled Hypertension (Systolic > 150, Diastolic > 90), 9. Untreated Hyperthyroidism, 10. Chronic Kidney Disease (EGFR < 60), 11. Current anticoagulant use, 12. Poorly controlled Type 2 diabetes (Hemoglobin A1c in last 3 months > 8.5%), 13. chronic Chronic opioid use, 14. Insulin depende [...] [...]
Secondary endpointsdetails revised at 2 of 2 entries
Study description+26 characters
[...] ic surgery including sleeve gastrectomy and gastric bypass. WeInvestigators will investigate the frequency of 7-day emergency departmen [...] sits with SDD after bariatric surgery (Aim 1). In addition, wethe investigators will compare total 30-day charges between participants who [...]
2025-06-05
Original filing
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 Details
NCT Number NCT07011628
Lead Sponsor Vanderbilt University Medical Center
Conditions Obesity and Obesity-related Medical Conditions, Bariatric Surgery
Enrollment 200 participants
Start Date 2026-10-01
Primary Completion 2027-10-01 (estimated)
Study Completion 2028-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-09-21