ClinicalTrials.Veeva

Menu

Hospital Discharge Following Bariatric Surgery by Telepresence Robot

H

Hospital de Clinicas de Porto Alegre

Status

Unknown

Conditions

Severe Obesity

Treatments

Procedure: telepresence discharge
Other: Conventional discharge

Study type

Interventional

Funder types

Other

Identifiers

NCT04203602
25656919.4.0000.5327

Details and patient eligibility

About

This is a non-inferiority randomized controlled trial aimed to compare the effectiveness and feasibility of performing the ward round using a telepresence robot vs. a face-to-face ward round to discharge patients after bariatric surgery.

Full description

This study is aimed to analyze the effectiveness and feasibility of performing the ward round using a telepresence robot (PadBot U, Inbot Technology Ltd, China), compared to the face-to-face ward round, for hospital discharge after bariatric surgery. Patients who underwent either laparoscopic Roux-en-Y gastric bypass or laparoscopic sleeve gastrectomy will be randomized to one of two groups: intervention group - who will be evaluated and discharged, on postoperative day (POD) 2, during ward rounds with the assistant team present, but the telepresent surgeon via robot; and control group - who will be evaluated and discharged, on POD 2, during ward rounds with the whole team physically present.

The study main hypothesis is that the ward rounds with the surgeon telepresent by a robot are not inferior to the face to face ward rounds, to evaluate and discharge patients after bariatric surgery.

Enrollment

96 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients that underwent bariatric surgery (either laparoscopic Roux-en-Y gastric bypass or laparoscopic sleeve gastrectomy

Exclusion criteria

  • complications during surgery; unable to sign informed consent; admitted to ICU; previous foregut surgery.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

96 participants in 2 patient groups

Telepresence round
Experimental group
Description:
Patients will be seen during ward rounds by the multidisciplinary team physically present, but with the surgeon remotely present via a telepresence robot.
Treatment:
Procedure: telepresence discharge
conventional round
Active Comparator group
Description:
Patients will be seen during ward rounds by the whole multidisciplinary team physically present, including the surgeon.
Treatment:
Other: Conventional discharge

Trial contacts and locations

1

Loading...

Central trial contact

Guilherme S Mazzini, MD, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems