CompletedNot Applicable

Propofol and Sevoflurane for Catheter-Related Bladder Discomfort

South Korea82 participantsStarted 2014-11

Plain-language summary

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

Who can participate

Age range19 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Catheter-related Bladder Discomfort

Timeframe: 1 hour postoperatively

Trial details

NCT IDNCT02252445

SponsorSeoul National University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-01

Results submitted2016-05-02

View on ClinicalTrials.gov More Catheter Site Discomfort trials