Gabapentin and CRBD
Phase 3
- Conditions
- Postoperative Catheter-related Bladder Discomfort in Patients Undergoing open prostatectomy.Mechanical complication of urinary (indwelling) catheter
- Registration Number
- IRCT2014063017811N4
- Lead Sponsor
- Arak University of Medical Science,Office of Vice Chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 42
Inclusion Criteria
inclusion criteria: Patients of American Society of Anesthesiologists (ASA) physical status I-II undergoing elective open prostatectomy surgery under spinal anesthesia ; requiring catheterization of the urinary bladder ; 50–80 kg of weight
exclusion criteria: Patients with history of OAB (urinary frequency >3 times at night and > 8 times in 24 hours) ; neurogenic bladder; diabetes mellitus ; Parkinson’s disease and impaired renal function ; chronic use of opiates or sedatives ; antiacid uptake in the past 48 hours ; hypersensitivity to amide local anesthetics or gabapentin
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Catheter-related bladder discomfort(CRBD) severity. Timepoint: at hours 2,5,24,48,72 after surgery. Method of measurement: based on asking patients based on Likert scale.;Pain severity. Timepoint: at hours 2,5,24,48,72 after surgery. Method of measurement: based on VAS index.
- Secondary Outcome Measures
Name Time Method Total morphine requirement. Timepoint: at hours 2,6,24,48,72. Method of measurement: counting amount of morphine that will be injected to patient.;Postoperative sedation. Timepoint: at hours 2,6,24,48,72. Method of measurement: clinical examination.;Postoperative N/V. Timepoint: at hours 2,6,24,48,72. Method of measurement: clinical examination and history taking.