Evaluation of Optimal Dose of Local Anesthetics for Patient Controlled Continuous Femoral Nerve Block

NCT01198340 — Not applicable, Unknown, 60 participants, Okayama University

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

Evaluation of Optimal Dose of Local Anesthetics for Patient Controlled Continuous Femoral Nerve Block With Sciatic Nerve Block After Total Knee Arthroplasty

RegistryNCT01198340
StatusUnknown
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, treatment
Enrollment60 (Estimated)
SponsorOkayama University (Other)
ConditionsArthropathy of Knee Joint
InterventionsPC-FNB with basal administration of local anesthetics, PC-FNB without basal local anesthetics (Procedure)
Datesstart 2010-09-01, primary completion 2012-03-01 (estimated), completion 2012-06-01 (estimated), first posted 2010-09-10, last updated 2011-07-22
Locations1 site in Japan

Related Papers Related Patents Related Grants Related Experts
All trials for Arthropathy of Knee Joint All trials of PC-FNB with basal administration of local anesthetics All trials of PC-FNB without basal local anesthetics

-Summary

To evaluate an analgesic effect without basal administration of local anesthetics for patient-controlled femoral nerve block (with sciatic nerve block) after total knee arthroplasty.

Expand all sections  ·  Collapse all

+Arms and interventions

ArmTypeInterventionsDescription
With basal local anestheticsActive comparatorProcedure: PC-FNB with basal administration of local anesthetics
Without basal local anestheticsExperimentalProcedure: PC-FNB without basal local anesthetics
  • PC-FNB with basal administration of local anesthetics (Procedure), also known as PC-FNB with basal ropivacaine administration: Administration of 0.2% ropivacaine for femoral nerve block with 3 ml/h of basal dose, 5ml bolus by the patient, 60 minutes of lock out time.
  • PC-FNB without basal local anesthetics (Procedure), also known as PC-FAB without basal ropivacaine administration: Administration of 0.2% ropivacaine for femoral nerve block without basal dose, with 8 ml bolus by the patient, 60 minutes of lockout time.

+Outcome measures

Primary outcomes

  • pain scores by use of numerous rating scale (NRS) [4 days after the surgery]

Secondary outcomes

  • dose of local anesthetics [4 days after the surgery]

+Eligibility

Sex: All, ages: 20 Years to any

Inclusion Criteria:

* patients older than 20 yrs old scheduled for total knee arthroplasty

Exclusion Criteria:

* none

+Locations (1)

FacilityCityCountryStatus
Anesthesiology and Resuscitology, Okayama University HospitalOkayama, Okayama-kenJapanRecruiting

+Investigators