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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 prostatectomy
N52.34
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
NameTimeMethod
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
NameTimeMethod
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