Viewing Study NCT04754165



Ignite Creation Date: 2024-05-06 @ 3:47 PM
Last Modification Date: 2024-10-26 @ 1:57 PM
Study NCT ID: NCT04754165
Status: RECRUITING
Last Update Posted: 2024-03-19
First Post: 2021-01-29

Brief Title: Postoperative VR for Recovery After Bariatric Surgery
Sponsor: Beth Israel Deaconess Medical Center
Organization: Beth Israel Deaconess Medical Center

Study Overview

Official Title: Postoperative Virtual Reality VR for Recovery After Bariatric Surgery
Status: RECRUITING
Status Verified Date: 2024-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The objective of this study is to investigate whether the addition of immersive virtual reality VR in the immediate postoperative period to an enhanced recovery after surgery ERAS protocol could improve postoperative recovery from bariatric surgery
Detailed Description: The investigators propose conducting a randomized controlled single-center clinical trial of patients recovering from laparoscopic bariatric surgery The objective is to investigate whether the use of virtual reality VR during the immediate postoperative period could improve patient reported quality of recovery and potentially reduce opioid analgesic requirements as compared to an existing ERAS protocol

The investigators hypothesize that immersive VR will improve subjective quality of recovery scores at time of Post Anesthesia Care Unit PACU discharge as compared to standard ERAS

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None