NCT00757198

Requirement of Analgesics After Two Remifentanil Dosing Regimen in Cardiac Surgery.

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 90 (actual)
• Sponsor: Kuopio University Hospital · Academic / Other
• Sex: All
• Age: 18 Years – 80 Years
• Healthy volunteers: Not accepted

Summary

Prospective double blind study comparing two remifentanil dosing protocols (0.1 and 0.3 mcg/kg/min) during cardiac surgery. Main outcome measures are postoperative opioid requirements (PCA oxycodone) and postoperative pain (VAS, verbal rating scale).

Conditions

• Pain

Interventions

Type	Name	Description
DRUG	remifentanil	remifentanil infusion
DRUG	remifentanil	remifentanil infusion

Timeline

• Start date: 2008-09-01
• Primary completion: 2011-11-01
• Completion: 2011-12-01
• First posted: 2008-09-23
• Last updated: 2013-09-12

Locations

1 site across 1 country: Finland