Survey the effect of pain control in patients with extremities trauma in triage room on the outcome and patients’ satisfaction

Effect of pain controlon patients’ satisfaction in patients with extremities trauma

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017020227457N3

Enrollment

100

Registered

2017-02-20

Start date

2017-02-19

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

extremities trauma. Transient arthropathy

Interventions

Intervention 1: Intervention group: control pain in triage room. Patients in the intervention group receive 0.05 mg/kg morphine sulfate. Intervention 2: Control group: Without control pain in triage r

Treatment - Drugs

Intervention group: control pain in triage room. Patients in the intervention group receive 0.05 mg/kg morphine sulfate.

Control group: Without control pain in triage room. Patients in control group received distilled water.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria included patients with extremity trauma. Exclusion Criteria included patients who have stomach ulcers and Mental diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Patient satisfaction of extremity trauma. Timepoint: After controlling pain. Method of measurement: Based on feedback from patients.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mehdi Rezaie

Iran University of Medical Sciences

rezaei.me@iums.ac.ir+98 216435210

Outcome results

None listed

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