A method of pain reduction during prostate biopsy
Phase 2
- Conditions
- Dysplasia of prostate.Dysplasia of Prostate, Low grade dysplasia
- Registration Number
- IRCT201612013773N17
- Lead Sponsor
- Vice chancellor for research of Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 96
Inclusion Criteria
Patients candidate for prostate biopsy; Minimum weight 40 kg
Exclusion criteria: uncontrolled blood pressure; sensitivity to local anesthetics; advanced heart, renal or hepatic disease; opioid addiction.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before and During Biopsy. Method of measurement: VAS Score.;Blood Pressure. Timepoint: Before and During Biopsy. Method of measurement: Monitoring.;Heart Rate. Timepoint: Before and During Biopsy. Method of measurement: Pulse Oximetry.
- Secondary Outcome Measures
Name Time Method evel of consciousness. Timepoint: Before and during biopsy. Method of measurement: Miller Score.