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Comparison of intravenous non-vented lidocaine effects in the relief of acute pain in extremity trauma patients

Not Applicable
Recruiting
Conditions
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Pain, unspecified
Registration Number
IRCT20180131038569N1
Lead Sponsor
Deputy of Research of Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
32
Inclusion Criteria

Patients with limb trauma require pain relief with NRS upper 5/10
age between16-65 years

Exclusion Criteria

dissatisfaction of patient from this study
Patient's allergy to lidocaine or morphine

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of pain. Timepoint: 0,10,20,30,60 minutes. Method of measurement: Numeric Pain Rating Scale.
Secondary Outcome Measures
NameTimeMethod
Systolic blood pressure. Timepoint: 0,10,20,30,60minutes. Method of measurement: MmHg.;Diastolic blood pressure. Timepoint: 0,10,20,30,60minutes. Method of measurement: MmHg.;Heart rate. Timepoint: 0,10,20,30,60minutes. Method of measurement: In a minute.;Respiratory rate. Timepoint: 0,10,20,30,60minutes. Method of measurement: In a minute.;O2 saturation. Timepoint: 0,10,20,30,60minutes. Method of measurement: percent.
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