Clinical trial Recruiting at 1 site Observational Ages 18 to 65

Early discharge with home hospital care after bariatric surgery

Official title: Economic Evaluation of an Early Discharge Pathway With Hospital-at-Home After Bariatric Surgery in Patients Undergoing Bariatric Surgery: A Comparative Observational Cohort Study

Run by Corporacion Parc Tauli · NCT07782281 · Data updated 2026-11-12

This study tests whether discharging patients 24 hours after bariatric surgery and following up with Hospital-at-Home care is safe and cost-effective compared with the traditional 48-hour hospital stay.

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Quick facts

Study typeObservational
Ages18 Years to 65 Years
SexAll
Enrollment300 (estimated)
SponsorCorporacion Parc Tauli
Academic / other
Locations1 site (Sabadell, Barcelona)
StatusRecruiting
StartedFebruary 15, 2025
Main results expectedJanuary 2028
Study endsJanuary 2028
Registry record updatedAugust 24, 2026
Trial IDNCT07782281 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years and older undergoing elective bariatric surgery who have complete data and meet the predefined study period criteria.

Probably not a fit

Patients with intraoperative complications, emergency surgery, or incomplete data may not benefit from the early discharge pathway.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an ambispective observational cohort study conducted in a real-world setting to compare two postoperative pathways after bariatric surgery: an early discharge model with 24 hours in hospital plus Hospital-at-Home care on the second day, versus the conventional 48-hour hospital stay. The evaluation focuses on direct healthcare costs, resource use, clinical safety, organizational efficiency, applicability, and patient satisfaction. Enhanced recovery protocols, minimally invasive techniques, and multimodal perioperative care are integral to the early discharge strategy. The study uses historical controls and prospective data from February 2025 onward at Hospital Universitari Parc Taulí to assess economic and organizational impact. Results are intended to inform whether Hospital-at-Home can safely substitute part of inpatient care without compromising outcomes.

Why it matters

Potential benefit: If successful, patients could benefit from shorter hospital stays, potential cost savings, and continued recovery at home with maintained safety and satisfaction.

How similar studies have gone: Previous studies in similar ERAS and Hospital-at-Home perioperative models have shown promise, but this exact early-discharge plus HaH approach after bariatric surgery is being evaluated in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or older.
* Patients undergoing elective bariatric surgery.
* Bariatric surgery performed during the predefined study periods for either cohort.
* Availability of sufficient clinical and economic data for study analysis.

Exclusion Criteria:

* Emergency surgery.
* Intraoperative complications requiring postoperative management outside the standard care pathway.
* Unplanned admission to an intensive care unit.
* Incomplete clinical or economic data preventing study analysis.

Where it's running

  • Hospital Universitari Parc Taulí
    Sabadell, Barcelona, Spain
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.