Clonidine efficacy in acute renal colic
Phase 3
- Conditions
- Acute renal colic.Unspecified renal colic
- Registration Number
- IRCT20130108012072N11
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Agreement for entering to the study
No Mental Retardation
Non pregnant
No breast feeding
Didn't use of analgesic agents since 4 hours ego
No sensitivity to Morphine or Ketorolac or Clonidine
Blood Pressure >=110/70 mm Hg
No history of chronic liver or kidney injury
VAS (Visual Analog Score)>4
Exclusion Criteria
Analgesic agents use since 4 hours ego
History of drug reaction
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity score with Visual Analog Scale. Timepoint: Study beginning, 20 minutes and 40 minutes after treatment. Method of measurement: Visual Analog Scale.;Drug complications. Timepoint: Study beginning, 20 minutes and 40 minutes after treatment. Method of measurement: Standard questionnaire form.
- Secondary Outcome Measures
Name Time Method Insufficient pain control. Timepoint: 40 minutes after treatment. Method of measurement: Visual Analog Scale.