Skip to main content
Clinical Trials/NCT02252445
NCT02252445
Completed
Not Applicable

Effect of Propofol and Sevoflurane on Postoperative Catheter-Related Bladder Discomfort

Seoul National University Hospital1 site in 1 country82 target enrollmentNovember 2014

Overview

Phase
Not Applicable
Intervention
Propofol
Conditions
Catheter Site Discomfort
Sponsor
Seoul National University Hospital
Enrollment
82
Locations
1
Primary Endpoint
Catheter-related Bladder Discomfort
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The investigators want to evaluate the efficacy of the propofol and sevoflurane for the prevention of catheter-related bladder discomfort.

Detailed Description

The mechanism of catheter-related bladder discomfort is thought to be related to the muscarinic receptor. Propofol and desflurane are most widely used as an anesthetic agent. Propofol and desflurane are known to block the muscarinic receptor in different ways. The investigators want to evaluate the efficacy of the propofol and sevoflurane for the prevention of catheter-related bladder discomfort.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
January 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for transurethral bladder excision under general anesthesia
  • ASA I-III

Exclusion Criteria

  • Foley catheter less than 18 Fr.
  • Patients with obstruction of urinary tract
  • Patients with neurogenic bladder
  • Patients with severe obesity
  • Patients with neurologic disorder
  • Patients with chronic pain
  • Patients with allergic history to propofol or sevoflurane

Arms & Interventions

Propofol

Propofol will be administered as the anesthetic maintenance agent.

Intervention: Propofol

Sevoflurane

Sevoflurane will be administered as the anesthetic maintenance agent.

Intervention: Sevoflurane

Outcomes

Primary Outcomes

Catheter-related Bladder Discomfort

Time Frame: 1 hour postoperatively

Catheter-related bladder discomfort will be measured at 1 hour postoperatively (0:none, 1:mild, 2:moderate, 3:severe). Patients with score \>0 will be counted.

Secondary Outcomes

  • Blurred Vision(0, 1, 6 and 24 hour postoperatively)
  • Dry Mouth(0, 1, 6 and 24 hour postoperatively)
  • Flushing(0, 1, 6 and 24 hour postoperatively)
  • Dizziness(0, 1, 6 and 24 hour postoperatively)
  • Catheter-related Bladder Discomfort(0, 6 and 24 hour postoperatively)
  • Hemodynamic Parameters(0, 1, 5, 10 minute postoperatively)
  • Nausea(0, 1, 6 and 24 hour postoperatively)
  • Vomiting(0, 1, 6 and 24 hour postoperatively)
  • Analgesics(0, 1, 6 and 24 hour postoperatively)

Study Sites (1)

Loading locations...

Similar Trials