Comparison of venous lidocaine with venous morphine in reducing acute pain due to trauma

Comparison of venous lidocaine efficacy with intravenous morphine in reducing acute pain in patients with trauma

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180805040712N2

Enrollment

Registered

2019-03-10

Start date

2017-12-27

Completion date

Unknown

Last updated

2019-03-25

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

Conditions

Patients with limb trauma.

Interventions

Intervention 1: Intervention group: The first intervention group will receive 0.1mg / kg morphine sulfate as a slow intravenous injection. Intervention 2: Intervention group: The second intervention g

Eligibility

Sex/Gender

All

Age

16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Acute upper or lower limb trauma including soft tissue injury Fractures as the main cause of referral Dislocation Need to get analgesia due to extreme pain in the limbs

Exclusion criteria

Exclusion criteria: Disorders of consciousness Hemodynamic Disorders During Injection Sensitization Lidocaine and Morphine

Design outcomes

Primary

Measure	Time frame
Intensity of pain. Timepoint: At the time of referral, then 15, 30, 45 and 60 minutes after the administration of the drug. Method of measurement: Using the numerical scale of pain assessment.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEsmaile raiyat dust

Jahrom University of Medical Sciences

navidkalani@gmail.com+98 71 5423 0085

Outcome results

None listed

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