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Evaluation of the success rate of hematoma block with and without ultrasound-guide in pain control of distal radial fracture reduction in patients presenting to the emergency department

Evaluation of the success rate of hematoma block with and without ultrasound-guide in pain control of distal radial fracture reduction in patients presenting to the emergency department

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016020126315N1
Enrollment
80
Registered
2016-06-04
Start date
2015-03-20
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

Fracture of the distal radius. Fracture of lower end of radius

Interventions

Intervention 1: In A group, hematoma block without ultrasound guidance, after disinfection, lidocaine 1% is injected in the center of the hematoma and around ulnar styloid with Barbutazh technique. Te
Diagnosis
In A group, hematoma block without ultrasound guidance, after disinfection, lidocaine 1% is injected in the center of the hematoma and around ulnar styloid with Barbutazh technique. Ten minutes after
In B group, hematoma block with ultrasound guidance, at first we identify hematoma with ultrasound and after disinfection, lidocaine 1% is injected in the center of the hematoma and around ulnar stylo

Sponsors

Mashhad University of Medical Sciences Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with acute fractures of the distal forearm ASA class I and II and among people over the age of 18 years Exclusion criteria: Older fractures than 12 hours; Open fractures due to technical problem; Patients with a history of drug abuse or any kind of debilitating CNS and respiratory medications

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: before block, 30 minutes after reduction. Method of measurement: visual analog scale.

Secondary

MeasureTime frame
Reducton time. Timepoint: reduction time. Method of measurement: minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Assiyeh Baradaran Fard

Mashhad University of Medical Sciences

assibfard@gmail.com; baradaranfa921@mums.ac.ir; pishbine@mums.ac.ir+98 51 3852 5312

Outcome results

None listed

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