Clinical Trials Directory

Trials / Completed

CompletedNCT06379490

Ultrasound-guided Infraclavicular Block With Lidocaine or Ropivacaine for Closed Reduction of Distal Radius Fractures

Effect of Ultrasound-guided Lateral Infraclavicular Brachial Plexus Block With Lidocaine or Ropivacaine for Closed Reduction of Distal Radius Fractures - A Randomized Controlled Non-inferiority Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
67 (actual)
Sponsor
Nordsjaellands Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To investigate the feasibility of the lateral infraclavicular plexus brachialis (LIC) block for acute closed reduction of distal radius fractures, the investigators will compare the pain-relieving and muscle-relaxing properties of the LIC block with short- and long-acting local anesthetics in different concentrations but at the same volume. In addition to motor and sensory blockade during repositioning, feasibility will also be assessed by other patient-related and block-related factors, as well as by factors related to the repositioning and plastering procedure.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0.2% Injectable Solution30 ml of Ropivacaine 0.2% = 60 mg ropivacaine
DRUGLidocaine epinephrine30 ml of Lidocaine 1% with 5 μg/ml epinephrine = 300 mg lidocaine + 150 μg epinephrine
DRUGRopivacaine 0.5% Injectable Solution30 mL of Ropivacaine 0.5% = 150 mg Ropivacaine

Timeline

Start date
2024-04-23
Primary completion
2025-06-18
Completion
2025-06-18
First posted
2024-04-23
Last updated
2025-06-26

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT06379490. Inclusion in this directory is not an endorsement.