Ketamine-propofol versus alfentanil-propofol for analgesia during cystoscopy
Phase 2
- Conditions
- pain.Pain localized to other parts of lower abdomen
- Registration Number
- IRCT201401313289N7
- Lead Sponsor
- Arak University of Medical Sciences, Vice Chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
Inclusion Criteria: Elective rigid cystoscopy; either diagnostic or therapeutic; age between 18 and 65.
Exclusion Criteria
Patients with allergy to ketamine, propofol, and alfenatnil; pregnancy; emergency cystoscopy; patients on psychiatric medications; alcoholics.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate. Timepoint: at time zero and then every 5 minutes. Method of measurement: Cardiac monitoring.;Systolic blood pressure. Timepoint: at time zero and then every 5 minutes. Method of measurement: Mercury sphygmomanometer.;Diastolic blood pressure. Timepoint: at time zero and then every 5 minutes. Method of measurement: Mercury sphygmomanometer.;Arterial O2 saturation. Timepoint: at time zero and then every 5 minutes. Method of measurement: Pulse oximeter.;Respiratory rate. Timepoint: at time zero and then every 5 minutes. Method of measurement: Cardiac monitoring.;Analgesia score. Timepoint: Two hours after cystoscopy. Method of measurement: Visual analog scale.;Sedation score. Timepoint: Two hours after cystoscopy. Method of measurement: Ramsay sedation score.
- Secondary Outcome Measures
Name Time Method