Evaluation of the analgesic effect of sufentanil and paracetamol in comparison with the combination of ketorolac and paracetamol in open prostatectomy surgery
Phase 2
Recruiting
- Conditions
- Open prostatectomy.Erectile dysfunction following simple prostatectomyN52.34
- Registration Number
- IRCT20171111037369N2
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 60
Inclusion Criteria
All patients candidate for open prostatectomy
Exclusion Criteria
usage of opioid, analgesic or psychiatric drugs
renal failure
hepatic diseases
gastrointestinal diseases
patient who have allergic history to opium, ketorolac, paracetamol
contraindications for spinal anesthesia
contraindications for general anesthesia
spinal anesthesia failure and convertion to general anesthesia
respiratory depression during IV-PCA infusion
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of postoperative pain. Timepoint: 4, 8, 12, 24, 36 and 48 hours after surgery. Method of measurement: Visual Analogue Scale.;Sedation. Timepoint: 4, 8, 12, 24, 36 and 48 hours after surgery. Method of measurement: Ramssay score.
- Secondary Outcome Measures
Name Time Method