Feasibility and Health-economic Evaluation of Remote Clinical Monitoring Enabling Same-day Discharge After Bariatric Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorJessa Hospital

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

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators