Comparison of intravenous ibuprofen and intravenous ketorolac in renal colic pain reductio
Phase 3
Recruiting
- Conditions
- nspecified renal colic.Unspecified renal colic
- Registration Number
- IRCT20150213021063N5
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 195
Inclusion Criteria
Patients with renal colic who present to the emergency department and their pain intensities are equal or greater than 7 out of 10
Exclusion Criteria
History of an allergic reaction to ASA or other NSAIDs (including asthma, skin reactions, anaphylaxis, or ...)
Known chronic kidney disease
Age below 18 or above 65 years
Weight below 50 kilograms
Peptic ulcer disease history
Gastrointestinal bleeding history
Suspected volume deficit (based on mucous membranes)
Any active bleeding
Bleeding diathesis
Using anticoagulant or antiplatelet drugs
Known heart failure
Pregnancy
Lactation
Systolic blood pressure lower than 100 mmHg
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: Before drug administration, 30, 60, and 120 minutes after drug administration. Method of measurement: Numeric rating scale.;Adverse events. Timepoint: Patients will be monitored continuously for adverse events since drug administration till patient discharge. Method of measurement: Specific occurred adverse event.;Patient's length of stay. Timepoint: At the time of patient discharge. Method of measurement: Minutes.
- Secondary Outcome Measures
Name Time Method