Clinical Trials Directory

Trials / Completed

CompletedNCT00210158

Intraoperative Nitrous Oxide and Postoperative Pain for Patients With Current Opioid Treatment

Effects of Intraoperative Nitrous Oxide on Postoperative Pain for Patients With Current Opioid Treatment After Vertebroplasty.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Institut Bergonié · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREAirPatients undergo long-term morphine treatment and vertebral cementoplasty. During the procedure, patients are ventilated with a mixture of air and oxygen.
PROCEDUREProtoxPatients undergo long-term morphine treatment and vertebral cementoplasty. During the procedure, patients are ventilated with a mixture of oxygen and nitrous oxide.

Timeline

Start date
2005-01-01
Primary completion
2006-12-31
Completion
2006-12-31
First posted
2005-09-21
Last updated
2025-09-09
Results posted
2025-09-09

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00210158. Inclusion in this directory is not an endorsement.