Viewing Study NCT06486168



Ignite Creation Date: 2024-07-17 @ 11:22 AM
Last Modification Date: 2024-10-26 @ 3:33 PM
Study NCT ID: NCT06486168
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-06-21

Brief Title: Incidence of Diaphragmatic Dysfunction After Non-Intubated Video-Assisted Thoracoscopic Surgery
Sponsor: GCS Ramsay Santé pour lEnseignement et la Recherche
Organization: GCS Ramsay Santé pour lEnseignement et la Recherche

Study Overview

Official Title: Incidence of Diaphragmatic Dysfunction After Non-Intubated Video-Assisted Thoracoscopic Surgery
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: DYNASTY
Brief Summary: The objective of this this single-center prospective longitudinal study is to evaluate the incidence of diaphragmatic dysfunction after non-intubated video-assisted thoracoscopic surgery NIVATS

Participant will be evaluated during surgery 2 hours and 24 hours after surgery
Detailed Description: This is a prospective longitudinal single-center study conducted on patients undergoing non-intubated video-assisted thoracoscopic surgery The main indications for this surgery are wedge resections pneumothorax repair and pleural biopsies with or without talc pleurodesis for pleural effusion

Except for the inclusion visit each patient will be evaluated twice 2 and 24 hours after the end of the surgical procedure The data from each evaluation will be recorded by the physician in the electronic CRF

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