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Citalopram in the Renal Colic Pain Relief Management

Not Applicable
Conditions
Renal Colic.
Unspecified renal colic
Registration Number
IRCT2014020812072N1
Lead Sponsor
Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
90
Inclusion Criteria

The inclusion criteria : an age range of 18-55; a clinical diagnosis of acute colicky pain; pain severity of 7-10 based on visual analogue scale (VAS) and patients’ written consent to participate in the study
The exclusion criteria : pregnancy or suspected of being pregnant; contraindication in relation to taking morphine and citalopram based on drug catalog; a history of dependence on opioids or Selective serotonin re-uptake inhibitors; receiving an analgesic during a 6-hour period before presentation; peritonitis or peritoneal symptoms and signs; any disease preventing communication and patient’s decision to leave the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Renal Colic. Timepoint: every 20 min for 3 times. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
Pain severity. Timepoint: every 20 min for 3 times. Method of measurement: Visual Analogue Scale.
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