NCT01437462

Sevoflurane, Propofol, Postoperative Pain

Postoperative Pain After Propofol Sevoflurane Anaesthesia: a Prospective, Randomized, Single-blinded Trial

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 168 (actual)
• Sponsor: Tampere University Hospital · Academic / Other
• Sex: Female
• Age: 18 Years – 69 Years
• Healthy volunteers: Not accepted

Summary

The impact of anaesthetic method (intravenous vs. inhalational) has been proposed, but not proven in a large-scale study. The researchers aim to provide an investigation that has sufficient power to clarify the potential effect of anaesthetic method on postoperative need of opioids. Sevoflurane and propofol will be compared.

Conditions

• Healthy Adults
• Gynecological Disease

Interventions

Type	Name	Description
DRUG	Sevoflurane	Sevoflurane inhalation anesthesia, sufficient amount to maintain adequate general anesthesia for surgery
DRUG	Propofol	Propofol intravenous anesthesia, sufficient amount to maintain adequate anesthesia during surgery

Timeline

• Start date: 2008-10-01
• Primary completion: 2013-03-01
• Completion: 2013-03-01
• First posted: 2011-09-21
• Last updated: 2013-04-10

Locations

1 site across 1 country: Finland