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2% Lidocaine Plus 0.5% Bupivacaine Versus 0.5% Bupivacaine in Brachial Block for Creation of Arteriovenous (AV) Fistula

M

Mahidol University

Status and phase

Unknown
Phase 4

Conditions

Infraclavicular Brachial Plexus Block

Treatments

Drug: Bupivacaine plus lidocaine
Drug: Bupivacaine 30 ml

Study type

Interventional

Funder types

Other

Identifiers

NCT00993746
si433/2009

Details and patient eligibility

About

Will the technique of adding lidocaine to bupivacaine fasten the onset of bupivacaine alone for infraclavicular brachial plexus block in end-stage renal disease (ESRD) patient?

Enrollment

90 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ESRD patient for AVF procedure
  • age >17 year
  • BMI 20-35 kg/m2
  • communicable

Exclusion criteria

  • BMI > 35 kg/m2 BMI < 20 kg/m2 หรือ BW < 35 kg
  • History of allergy to local anesthetic drugs
  • Pre-operative neurological deficit, Neuromuscular disorder หรือ old CVA
  • Psychiatric disorder
  • Coagulation disorder
  • Uncontrolled seizure
  • Pregnant and lactating women

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

90 participants in 2 patient groups

Bupivacaine plus lidocaine
Active Comparator group
Description:
Group 1: bupivacaine 20 ml plus lidocaine 10 ml
Treatment:
Drug: Bupivacaine plus lidocaine
Bupivacaine alone
Experimental group
Description:
Group 2: bupivacaine 30 ml
Treatment:
Drug: Bupivacaine 30 ml

Trial contacts and locations

1

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Central trial contact

Orawan Pongraweewan, MD,FRCA

Data sourced from clinicaltrials.gov

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