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Intravenous fentanyl vs. erector spinae block in chest trauma pain

Acheiving analgesia in chest trauma related pain in the emergency department: intravenous fentanyl or ultrasound guided erector spinae block

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131226015941N7
Enrollment
60
Registered
2019-05-12
Start date
2019-05-22
Completion date
Unknown
Last updated
2019-05-21

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

Conditions

Unspecified injury of thorax (chest trauma). unspecified injury of thorax

Interventions

Intervention 1: Intervention group: Erector spinae fascial plain block will be performed under the real time vision by the ultrasound device (Mindray, 2012, China) and after proper sterile preparation
tissue expansion is checked by ultrasound in the time of injection. Intervention 2: Control group: Intravenous fentanyl (Caspiantamin, Iran) will be administered by slow injection (during 2 minutes) u

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over 16 years of age presenting to the emergency department with chest trauma initial pain score over 5 (from 10)

Exclusion criteria

Exclusion criteria: presence of distracting injuries impaired consciousness hypersensitivity to lidocaine or fentanyl presence of coagulopathy presence of any sensory impairment like peripheral neuropathy receiving pain killers before enrollment those who are not willing to participate or to continue their cooperation need for surgical intervention through the chest wall (including tube thoracostomy)

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: 20 minutes and 1 hour after injection or block. Method of measurement: asking the patient by numeric rating scale.

Secondary

MeasureTime frame
Total dose of intravenous fentanyl administered to achieve adequate analgesia. Timepoint: The first 6 hours of admission in the emergency department. Method of measurement: recording by the investigator.;Adverse reactions of the intervention(s). Timepoint: at the discharge time. Method of measurement: assessment by the investigator.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhossein Mirafzal

Kerman University of Medical Sciences

mirafzal@kmu.ac.ir+98 34 3223 5011

Outcome results

None listed

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