Viewing Study NCT03652324



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Last Modification Date: 2024-10-26 @ 12:53 PM
Study NCT ID: NCT03652324
Status: COMPLETED
Last Update Posted: 2018-08-31
First Post: 2018-08-28

Brief Title: What Should be the Anesthesia Method in Endobronchial Coil Treatment
Sponsor: TC Erciyes University
Organization: TC Erciyes University

Study Overview

Official Title: Comparison of General Anesthesia and Deep Sedation in Enbronchial Coil Treatment
Status: COMPLETED
Status Verified Date: 2018-08
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: This prospective randomize study was conducted in a university hospital Bronchoscopic lung volume reduction BLVR coil treatment has recently been introduced into clinical practice as an alternative for patients chronic obstructive pulmonary disease COPD with severe refractory heterorogenous emphysema to conventional medical treatment Thirty two patients diagnosed with COPD with severe refractory heterorogenous emphysema undergoing BLVR coil treatment were included in the study Seventeen procedure were performed under general anesthesia and fifteen procedure were performed under deep sedation-analgesia in the general anesthesia group peak pressure air leakage and end-tidal carbon dioxide were recorded In the both groups pulse oximeter transcutaneous carbondioxide recovery time bronchospasm laryngospasm pneumothorax massive bleeding were recorded
Detailed Description: None

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