Clinical Trials Directory

Trials / Terminated

TerminatedNCT00712517

Propofol Versus Volatile Anesthesia in Post Operative Pain Management

Do Patients Anesthetized With Propofol Have Less Pain Than Those Anesthetized With Volatile?

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
The Cleveland Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study will test the hypothesis that patients anesthetized with propofol suffer less postoperative pain than those anesthetized with sevoflurane.

Detailed description

Patients undergoing s stripping operation for varicose veins will be randomized to one of two groups. Group 1 patients will receive propofol anesthesia. Group 2 patients will receive sevoflurane anesthesia. Intraoperative measurements including mean-arterial pressure, heart rate, propofol infusion rate, remifentanil infusion rate, and end-tidal sevoflurane concentration will be taken at 15 minute intervals. Patients in both groups will receive Piritramid as necessary to control pain either intravenously or through patient controlled pump. VAS pain score, mean-arterial pressure, heart rate, nausea will be evaluated at 30 minute intervals during the first four postoperative hours. Piritramid dosage and vomiting will be recorded through the first postoperative morning. Patients will rate pain based on the VAS score for the period between leaving the recovery room and the first postoperative morning

Conditions

Interventions

TypeNameDescription
DRUGpropofolpropofol anesthesia 3-5mg/kg
DRUGsevofluranesevoflurane anesthesia

Timeline

Start date
2010-09-01
Primary completion
2014-05-01
Completion
2014-05-01
First posted
2008-07-10
Last updated
2016-07-20

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT00712517. Inclusion in this directory is not an endorsement.