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Ultrasound Guided Hematoma Block in Distal Radius Fractures

Not Applicable
Recruiting
Conditions
Fracture Dislocation
Dislocated Wrist
Dislocated Radius
Distal Radius Fractures
Interventions
Procedure: Blind hematoma block
Device: Ultrasound guided hematoma block.
Registration Number
NCT06193915
Lead Sponsor
Medical Centre Leeuwarden
Brief Summary

This study will investigate the effectiveness of analgesia of ultrasound hematoma block compared to 'blind' hematoma block in patients with dislocated distal radius fracture.

Detailed Description

Distal radius fractures represent one of the most common injuries in the Emergency Department (ED). Proper treatment especially for dislocated fractures can minimize the chance of residual injury. For closed reduction anesthesia is essential for safety, satisfaction and result. Different methods of regional anesthesia can be used but hematoma block (HB) is the technique most often used in EDs in the Netherlands and recommended by Dutch guidelines. In practice however a HB, does not always lead to adequate anesthesia, this might be because of poor infiltration into the fracture site. Ultrasound could additionally provide real-time guidance of injection into the fracture site, maximizing the analgesic effect of HB. In this study the effectiveness of analgesia of ultrasound HB will be compared to 'blind' HB in patients with a dislocated distal radius fracture.

Patients with a confirmed dislocated fracture of the distal radius requiring closed reduction will be randomized to either ultrasound guided hematoma block or normal 'blind' hematoma block. NRS-scores will be given before, during and after hematoma block and during and after reduction of the fracture. These scores will be the primary endpoint of this study.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Age ≥ 16 years

  • Confirmed fracture of the distal radius requiring closed reduction, defined as any off the following items(7):

    • >10 degrees of dorsal angulation;
    • >20 degrees of volar angulation;
    • >2 mm step-off intra-articular;
    • >3 mm radial shortening;
    • >15 degrees radial inclination;
    • Translation and non-intact radio-carpal alignment in the lateral view
    • Significant translation in the posterior-anterior(PA)-view.
Exclusion Criteria
  • No informed consent can be given (cognitive impairment, severe dementia, no knowledge of Dutch language e.a.)
  • Neurovascular compromise or open fractures requiring (immediate) surgery or reduction.
  • First reduction already performed
  • Multi-trauma patients requiring other urgent procedures/tests or with respiratory or hemodynamical compromise
  • Pre-existent osteosynthesis material in situ in the affected arm
  • Skin injury (with exception of minor abrasions), local infection or recent burns hindering or contra-indicating the use of ultrasound and ultrasound gel
  • Allergy for local anesthetics

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Blind hematoma blockBlind hematoma blockPatients in this group will receive standard treatment; hematoma block with palpation of the fracture site (blind hematoma block)
Ultrasound guided hematoma blockUltrasound guided hematoma block.Patients in this group will receive ultrasound guided hematoma block before reduction of their dislocated distal radius fracture.
Primary Outcome Measures
NameTimeMethod
Effectiveness of analgesia during closed reduction of a distal radius fractureNRS before, during and after (10-15 min) injection of hematoma block, NRS-score during closed reduction and after closed reduction (5 min)

Pain reduction will be measured on a Numeric Rating Scale( NRS-scale; 0-10) at different moments

Secondary Outcome Measures
NameTimeMethod
Number of participants in which hematoma was aspirated during hematoma blockDuring hematoma block

Measure of correct position of hematoma block if there is aspiration of blood (yes/no)

Procedural time of the reductionFrom moment physician is ready to start the reduction until cast is applied (up to maximum of 30 min.)

Time needed to perform reduction of the fracture

Procedural time of the Hematoma blockTime from insertion of the needle until needle is withdrawn out of the patient (up to maximum of 30 min.)

Time needed to perform HB (blind or ultrasound-guided; from moment of localization of the fracture until the moment the needle is out of the patient)

Satisfaction of reduction provided by physician performing reduction measured10-15 minutes after closed reduction

measured on a 5-points Likert-scale (Very satisfied, Somewhat satisfied, Neither satisfied nor dissatisfied, Somewhat dissatisfied or Very dissatisfied)

Satisfaction of the nurse for procedure and reduction10-15 minutes after closed reduction

measured on a 5-points Likert-scale (Very satisfied, Somewhat satisfied, Neither satisfied nor dissatisfied, Somewhat dissatisfied or Very dissatisfied)

Years of experience of treating physician with use of ultrasound.(up to) 10-15 minutes after last closed reduction attempt

Years of experience of treating physician with use of ultrasound.

Satisfaction of the patient for procedure and reduction10-15 minutes after closed reduction

measured on a 5-points Likert-scale (Very satisfied, Somewhat satisfied, Neither satisfied nor dissatisfied, Somewhat dissatisfied or Very dissatisfied)

Number of reductions(up to) 10-15 minutes after last closed reduction attempt

Defined as attempt(s) to align fracture and application of cast

Satisfaction of the HB provided by physician performing the HB procedure10-15 minutes after hematoma block

measured on a 5-points Likert-scale (Very satisfied, Somewhat satisfied, Neither satisfied nor dissatisfied, Somewhat dissatisfied or Very dissatisfied)

Number of patients in which palpation of an evident step-off near fracture site was feltDuring performing hematoma block

Before performing hematoma block performing physician will palpate if there is a clear step-off near the fracture site (important especially in blind hematoma group)

Years of experience of treating physician in performing HB.(up to) 10-15 minutes after last closed reduction attempt

Years of experience of treating physician in performing HB.

Trial Locations

Locations (1)

Medisch Centrum Leeuwarden

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Leeuwarden, Friesland, Netherlands

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