Viewing Study NCT00210158



Ignite Creation Date: 2024-05-05 @ 12:02 PM
Last Modification Date: 2024-10-26 @ 9:18 AM
Study NCT ID: NCT00210158
Status: COMPLETED
Last Update Posted: 2013-07-26
First Post: 2005-09-12

Brief Title: Intraoperative Nitrous Oxide and Postoperative Pain for Patients With Current Opioid Treatment
Sponsor: Institut BergoniƩ
Organization: Institut BergoniƩ

Study Overview

Official Title: Effects of Intraoperative Nitrous Oxide on Postoperative Pain for Patients With Current Opioid Treatment After Vertebroplasty
Status: COMPLETED
Status Verified Date: 2007-10
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: PROTOX
Brief Summary: Peroperative opioids are known to induce N-Methyl-D-Aspartate dependent enhancement of postoperative hyperalgesia For patients with current opioid treatment these phenomena could be exagerated and could produce greater postoperative opioid consumption and higher pain score Since Nitrous oxide has anti- N-Methyl-D-Aspartate properties the aim of this study was to evaluate in patients with current opioid treatment the effects of peroperative Nitous oxide on postoperative opioid consumption and pain score after vertebroplasty
Detailed Description: None

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
Secondary IDs
Secondary ID Type Domain Link
PROTOX None None None