Viewing Study NCT06518239



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06518239
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-06-12

Brief Title: Establishing Optimal PEEP Setting for Obese Patients in the Steep Trendelenburg Position
Sponsor: None
Organization: None

Study Overview

Official Title: Establishing Optimal PEEP Setting for Obese Patients in the Steep Trendelenburg Position a Pilot Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine whether the Enlight 2100 electrical impedance tomography EIT belt can optimize positive end-expiratory pressure PEEP during surgery better than standard anesthesia machines
Detailed Description: Positive end-expiratory pressure PEEP is a measure taken intraoperatively to manage breathing during surgery The Enlight 2100 is a device that uses electrical impedance tomography EIT to measure PEEP and provide a live image of the lungs while a patient is mechanically ventilated In this study the investigators will use the Enlight 2100 EIT belt to measure PEEP intraoperatively in order to better optimize PEEP settings for difficult cases

Study Oversight

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