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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180131038569N1
Enrollment
32
Registered
2018-04-12
Start date
2017-08-23
Completion date
Unknown
Last updated
2018-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

??? ??? ?? ???????. Pain, unspecified

Interventions

Intervention 1: Intervention group: Lidocaine nebulizer is administered at a dose of 10 mg / kg and is administered intravenously to placebo (distilled water 0.1 cc / kg) for patients. Intervention 2:

Sponsors

Deputy of Research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: 0,10,20,30,60 minutes. Method of measurement: Numeric Pain Rating Scale.

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehzad Sadeghi ?Amroabadi

Deputy of Research of Tehran University of Medical Sciences

B.s1367@yahoo.com+98 21 61111

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026