Comparison of the analgesic efficacy of pethedine and ketorolac in renal colic patients
Phase 2
Recruiting
- Conditions
- Investigation of pain in renal colic patients.Diseases of the genitourinary system
- Registration Number
- IRCT20221229056978N1
- Lead Sponsor
- Ilam University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 108
Inclusion Criteria
All renal colic patients who have been confirmed by clinical and laboratory diagnosis
Exclusion Criteria
Women who are pregnant
Breastfeeding mothers
Patients who received sedation less than 6 hours before arrival
People with kidney dysfunction
Patients treated with warfarin
Patients with gastrointestinal disorders after taking NSAIDs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain level of renal colic patients. Timepoint: Pain measurement before the start of the intervention in all three groups, upon arrival and 35 minutes in the pethidine group, upon arrival and 3 minutes in the ketorolac group, and upon arrival and 35 minutes in the combination solution group of ketorolac and pethidine. Method of measurement: The method of measurement of the qualitative study is based on the functional status as follows: Weak impairment: able to return to work and drive a car 2_Mild impairment: able to perform daily activities at home 3_Severely injured: confined to bed.
- Secondary Outcome Measures
Name Time Method