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Erector spinae block vs. intercostal nerve block in thoracic trauma

Ultrasound guided erector spinae block vs. ultrasound guided intercostal nerve block for thoracic trauma pain management in the emergency department

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131226015941N9
Enrollment
76
Registered
2021-01-16
Start date
2021-02-03
Completion date
Unknown
Last updated
2021-02-22

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) The block will be performed by a se
tissue expansion is checked by ultrasound in the time of injection. Intervention 2: Control group: Intercostal nerve block will be performed under the real time vision by the ultrasound device (Mindra
this procedure is repeated for 2 ribs upper and 2 ribs lower than the first site with 3-4 ml of 1% Lidocaine.

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: ?All adult patients with thoracic trauma initial pain score over 5 using numeric pain scale (0-10)

Exclusion criteria

Exclusion criteria: Distracting injuries Altered mental status Any contraindications to Lidocaine Need for tube thoracostomy or thoracic surgery Impaired pain perception (Neuropathies, etc.) Large painful area (which can not be managed using intercostal nerve block) Patient refusal to participate

Design outcomes

Primary

MeasureTime frame
Pain score (using numeric rating scale) 20 minutes following the procedures. Timepoint: Twenty minutes following the procedures. Method of measurement: Asking the patient.;Pain score minutes following the procedures. Timepoint: Sixty minutes following the procedures. Method of measurement: Asking the patient.;Total fentanyl dose administered. Timepoint: Six hours following admission. Method of measurement: Physician order and Nurse report.

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