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Effect of oral ketamine versus placebo on pain relief in patients with renal colic

Phase 2
Conditions
Renal colic.
Unspecified renal colic
Registration Number
IRCT201410319014N46
Lead Sponsor
Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
44
Inclusion Criteria

(a) having renal colic; (b) age of 18 to 60 years.
Exclusion criteria: (a) having psychological or personality disorder; (b) pregnancy or breastfeeding; (c) having cardiovascular diseases, hypertension, epilepsy, glaucoma, or diabetes.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of pain. Timepoint: before and 3 hours after intervention. Method of measurement: using Visual Analog Scale.
Secondary Outcome Measures
NameTimeMethod
Severity of nausea. Timepoint: before and 3 hours after intervention. Method of measurement: using Four Point Scale.;Number of vomiting. Timepoint: before and 3 hours after intervention. Method of measurement: with question.
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