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USG Brachial Plexus Block for Upper Extremity Surgery

J

Jens Borglum Neimann

Status

Completed

Conditions

Fracture at Wrist and/or Hand Level
Injuries to the Wrist, Hand and Fingers (S60-S69)
Carpal Tunnel Syndrome
Ganglion Cysts
Rupture of Tendon of Wrist and Hand

Treatments

Drug: Ropivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01993290
BBH-PB
H-2-2012-055 (Other Identifier)

Details and patient eligibility

About

Ultrasound-guided (USG) brachial plexus (BP) block efficacy at the Supraclavicular (SCL), Lateral- Infraclavicular (LIC) and Axillary (AX) level: Randomized, observer-blinded study of the single-penetration multiple-injection-technique.

Full description

The investigators will compare the BP block efficacy (for surgical anaesthesia) with the USG single-penetration multiple-injection-technique at the SCL, LIC and AX level for upper-extremity surgery (elbow, forearm, wrist, hand). The investigators want to investigate whether the single-penetration multiple-injection-technique would provide for safe surgical anaesthesia with lower volumes of local anaesthetics than has previously been described in a comparative study at the three different levels.

120 patients will prospectively be randomized to an USG BP block administered as a single-penetration multiple-injection-technique at one of three different levels: (1) SCL (2) LIC (3) AX. Ropivacaine 0.75% (20 mL) will be used for all blocks prior to surgery.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age above 18 years
  • American Society of Anaesthesiology class 1-3
  • Patients undergoing upper extremity surgery

Exclusion criteria

  • Inability to cooperate
  • Inability to understand and talk danish
  • Allergic to ropivacaine
  • Infection at site of surgery
  • Neurological dysfunction at site of surgery
  • Severe coagulopathy
  • Drug and alcohol abuse
  • Patients, who can not get a nerve block due to technical difficulty
  • Pregnancy or nursing
  • Body mass index >35

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

120 participants in 3 patient groups

USG Supraclavicular block
Active Comparator group
Description:
20 ml of ropivacaine 0,75% is administered to brachial plexus at supraclavicular level.
Treatment:
Drug: Ropivacaine
Lateral infraclavicular block
Active Comparator group
Description:
20 ml of ropivacaine 0,75 % is administered to brachialis plexus at lateral infraclavicular level
Treatment:
Drug: Ropivacaine
USG Axillaris block
Active Comparator group
Description:
20 ml of ropivacaine 0,75% is administered to plexus brachialis at axillaris level
Treatment:
Drug: Ropivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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