CompletedPhase 2/3

Effect of Pregabalin Administration on Catheter- Related Bladder Discomfort in Urological Surgical Operations

Greece78 participantsStarted 2017-07-28

Plain-language summary

The aim of this study is to assess the effect of pregabalin administration on catheter-related bladder discomfort (CRBD). The study group includes patients that are about to be subjected to urological operations because of the high incidence of CRBD observed in this kind of surgical population.

Who can participate

Age range45 Years – 85 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * All patients about to be subjected to urinary operations * Signed informed consent Exclusion Criteria: * Preoperative urinary bladder/kidney dysfunction as a result of spinal cord pathology * History of overactive ((urinary frequency\>3 times at night and \>8 times in 24 hours), neurogenic bladder * End stage renal failure * Central nervous system dysfunction * Mental illness/ substance abuse * Sensitivity to pregabalin * Preoperative administration of pregabalin for other indications * Recent bladder catheterization \<3 months

What they're measuring

Percentage of postsurgical catheter-related bladder discomfort after preoperative pregabalin administration

Timeframe: Change from preoperative status to postoperative one at 0, 1, 2, 6, 24 hours postoperatively

Trial details

NCT IDNCT03229668

SponsorSaint Savvas Anticancer Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-12-31

View on ClinicalTrials.gov More Pregabalin on Catheter Related Bladder Discomfort trials