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Plasma Concentrations of Bupivacaine After Peri-articular Injection in Total Knee Arthroplasty

M

Mahidol University

Status and phase

Completed
Phase 4

Conditions

Serum Bupivacaine Level
Total Knee Arthroplasty
Periarticular Block

Treatments

Drug: Bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01636869
010/2555

Details and patient eligibility

About

Patients with knee arthroplasty usually performed under spinal anesthesia with a single-shot femoral nerve block and periarticular block, so we would like to know the plasma concentration of bupivacaine in these patients.

Enrollment

43 patients

Sex

All

Ages

30 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age of 30-70 yr
  • ASA I-II
  • patient undergo total knee arthroplasty under spinal block and single shot femoral nerve block and periarticular block

Exclusion criteria

  • patient's refusal
  • allergic to bupivacaine
  • body weight less than 50 kg
  • liver disease
  • heart disease
  • coagulopathy
  • Hct<35%
  • infection at both groin

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

43 participants in 1 patient group

bupicavaine
Experimental group
Treatment:
Drug: Bupivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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