WithdrawnPhase 2/3

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

Stopped: All patients during the study period were subjected to peripheral blocks or were excluded from the study due to exclusion criteria

Greece0Started 2017-08-16

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 orthopedic operations.

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 IDNCT03232021

SponsorSaint Savvas Anticancer Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-12-31

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