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The effect of single dose Nefopam on postoperative catheter-related bladder discomfort in patients undergoing transurethral resection of prostate: A randomized controlled trial

Phase 4
Recruiting
Conditions
catheter related bladder discomfort
normal saline 100 ml intravenous drip in 30 min
Registration Number
TCTR20191217005
Lead Sponsor
Faculty of Medicine, Khon Kaen University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
74
Inclusion Criteria

Patient undergoing Transurethral resection of prostate (TUR-P) under spinal anesthesia
ASA physical status class I-III
able to make decision and communicate
on urinary catheter traction at least 12 hours after operation

Exclusion Criteria

known allergic to nefopam or morphine
epilepsy
heart failure
arrhythmia
liver disease (total bilirubin>1.2 mg/dl AST>80 U/L ALT>66 U/L ALP>240 U/L)
Chronic kidney disease (GFR<60 ml/min/1.73 cm3)
current usage of monoamine oxidase inhibitor
drug abuse, alcoholism
acute closed angle glaucoma
morbid obesity (BMI>40 kg/m2)
psychological illness
chronic pain

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
degree of catheter&#45;related bladder discomfort at 6 hour after operation patient report
Secondary Outcome Measures
NameTimeMethod
morphine consumption 24 hour after operation medical record
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