Pheniramine and catheter-related bladder discomfort
Not Applicable
- Conditions
- Neoplasms
- Registration Number
- KCT0004880
- Lead Sponsor
- Korea University Anam Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 76
Inclusion Criteria
1. Patients scheduled transurethral bladder resection or transurethral prostate resection under general anesthesia with informed consent
2. Patients aged 19-80 years with Americal Society of Anesthesiologists physical status classification system I-III
Exclusion Criteria
1. Patients who does not consent to the trial
2. Pregnancy
3. Patients with foley catheter (<18 Fr.)
4. Patients with the obstruction of urinary tract
5. Patients with overactive, neurogenic bladder
6. Patients with body mass index > 35 kg/m2
7. Patients with analgesic usage due to chronic pain
8. Patients with hypersensitivity to chlorpheniramine
9. Patients with seizure
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Catheter-related bladder discomfort at postoperative 1 hour
- Secondary Outcome Measures
Name Time Method Hypotension in the postanesthesia care unit;Catheter-related bladder discomfort at postoperative 6, 24 hour;Suprapuvic pain;Nausea;Vomiting;Dry mouth;Flushing;Dizziness;Blurred vision;Sedation scale