The effect of intravenous acetaminophen compared to intravenous morphine in reducing pain in trauma patients

Investigating the effect of intravenous acetaminophen compared to intravenous morphine in reducing pain in limb trauma patients: a double-blind randomized controlled clinical trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190618043934N26

Enrollment

Registered

2024-06-29

Start date

2024-07-22

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

trauma. Acute pain due to trauma

Interventions

Intervention 1: Intervention group: Intervention group 1: The group receiving morphine (Darou Pakhsh Pharmaceutical Company - Iran) with a dose of 0.1 mg/kg once intravenously is slow. Intervention 2:

Eligibility

Sex/Gender

All

Age

15 Years to No maximum

Inclusion criteria

Inclusion criteria: Informed consent to enter the study Age above 15 years

Exclusion criteria

Exclusion criteria: Allergy to morphine or acetaminophen Addiction Use of painkillers before going to the emergency room Need for surgical intervention Non-cooperation for the study Personal satisfaction

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: The level of pain is evaluated first, 5, 15 and 30 minutes after receiving the medicine. Method of measurement: Using of Visual Analogue Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZabihullah Mohaqiq

Birjand University of Medical Sciences

zabihullahmohaghegh@gmail.com+98 56 3232 3232

Outcome results

None listed

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