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The effect of inhaled salbutamol on the pain intensity of patients with problems caused by acute renal colic: A double-blind clinical trial study.

Phase 1
Recruiting
Conditions
Acute renal colic.
Unspecified renal colic
Registration Number
IRCT20231205060266N1
Lead Sponsor
Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Pain intensity based on Visual Analog Scale (VAS) in the medium range
The patient's willingness to participate in the study and obtain informed consent
The presence of clinical symptoms of renal colic along with at least one of the three cases of hematuria in the complete urine analysis test, seeing stones in radiography or ultrasound of the urinary tract.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of patients' pain. Timepoint: Measurement of pain intensity before the intervention, and at intervals of 10, 20, 30, 45, 60 and 120 minutes after the intervention. Method of measurement: Evaluation of pain intensity with Visual Analog Scale (VAS), evaluation of hemodynamic variables with monitoring device.
Secondary Outcome Measures
NameTimeMethod
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