CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 82 enrolled
Drug / intervention
Propofol +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02252445
NCT02252445N/ACompleted
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Effect of Propofol and Sevoflurane on Postoperative Catheter-Related Bladder Discomfort

Seoul National University Hospital·interventional·Posted Sep 30, 2014·Updated Sep 1, 2016

In Brief

A clinical study evaluating Propofol and Sevoflurane for Catheter Site Discomfort and 3 related conditions. Completed, enrolled 82 participants across 1 site.

Detailed Summary

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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCatheter Site Discomfort, Complications, Anesthesia, Urinary Bladder Neoplasms
CountriesSouth Korea
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedSep 30, 2014
Enrollment StartNov 1, 2014
Primary CompletionJan 1, 2015
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 11.8 years ago

Interventions

Propofoldrug

Propofol will be administered.

Sevofluranedrug

Sevoflurane will be administered.