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A Retrospective Investigation of Local Anesthetic Concentrations in Femoral Nerve Block

G

Giorgio Veneziano

Status

Completed

Conditions

Postoperative Pain

Treatments

Procedure: Femoral nerve block with ropivacaine or bupivacaine

Study type

Observational

Funder types

Other

Identifiers

NCT02501135
IRB 15-00396

Details and patient eligibility

About

The purpose of this study is to retrospectively compare perioperative pain relief and safety in pediatric patients who have received a femoral nerve block with varying concentrations of local anesthetic.

Enrollment

281 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA physical status I or II
  • Age < or equal to 18 years of age at time of femoral nerve block
  • Femoral nerve block performed from 2010-2015

Exclusion criteria

  • ASA physical status > II
  • Co-morbid diseases (cardiac, pulmonary, neurological disease)
  • Use of adjunctive medications in femoral nerve block (except for epinephrine), such as dexamethasone

Trial design

281 participants in 1 patient group

Femoral Nerve Blocks
Description:
Patients who receive ropivacaine or bupivacaine during femoral nerve block.
Treatment:
Procedure: Femoral nerve block with ropivacaine or bupivacaine

Trial documents
1

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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