MedTrace Logo

Propofol and Sevoflurane for Catheter-Related Bladder Discomfort

NCT02252445 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2016-09-01

Study results available
· View outcomes & findings →

Summary

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

Conditions

  • Catheter Site Discomfort
  • Complications
  • Anesthesia
  • Urinary Bladder Neoplasms

Interventions

DRUG

Propofol

Propofol will be administered.

DRUG

Sevoflurane

Sevoflurane will be administered.

Sponsors & Collaborators

  • Seoul National University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2015-01-31
Completion
2015-01-31

Countries

  • South Korea

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02252445 on ClinicalTrials.gov