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Ultrasound-guided Supraclavicular Brachial Plexus Block in Elderly (US-SCB)

Š

Šarić, Jadranka Pavičić, M.D.

Status

Completed

Conditions

Arm Injuries
Anesthesia

Treatments

Device: Elderly population, Middle aged population

Study type

Interventional

Identifiers

NCT01467596
EudraCT 2011-005432-26

Details and patient eligibility

About

The aim of this study is to determine the minimum effective volume of local anesthetic (50:50 mixture of 0.5% levobupivacaine and 2% lidocaine) required to produce an effective US-SCB for surgical anesthesia in 50% of patients and to calculate the effective volume required to produce an effective US-SCB in 95% of the patients (MEAV95) in elderly group (>65 years) and in middle aged group (<45years) of patients.

Full description

We believe that known data regarding the minimum anesthetic volume required for effective US-SCB from middle age population can not be applicable to the elderly population since our preliminary data, presented at Euroanesthesia meeting in Amsterdam, 2011, and published in abstract form in the European Journal of Anaesthesiology, showed that involutional changes of brachial plexus in elderly, assessed by measuring the cross-sectional area (CSA) of brachial plexus at the first rib, allowed a 35% reduction in local anesthetic volume for an effective US-SCB for surgical anesthesia in elderly patients in comparison with the younger patients.

Enrollment

44 patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA 1 - 3 elderly patients (>65 years) scheduled for hand surgery
  • ASA 1-3 middle aged patients (<45 years)

Exclusion criteria

  • Cognitive impairment
  • Coagulopathy
  • Allergy to local anesthetics
  • Infection at the puncture site,
  • Body mass index > 35 kg/m2

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

44 participants in 2 patient groups

Elderly population
Experimental group
Description:
MEAV50, MEAV95 Onset and duration of sensory and motor blockade
Treatment:
Device: Elderly population, Middle aged population
Middle aged population
Active Comparator group
Description:
MEAV50, MEAV95 Onset and duration of sensory and motor blockade
Treatment:
Device: Elderly population, Middle aged population

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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