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Femoral Nerve Block for Analgesia After Anterior Cruciate Ligament Reconstruction (FNB for ACLR)

M

Mahidol University

Status and phase

Completed
Phase 4

Conditions

Analgesia After ACL Reconstruction

Treatments

Drug: 0.25% Bupivacaine
Drug: 0.5% Bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01593566
Mahidol University

Details and patient eligibility

About

Femoral nerve block using 0.25% bupivacaine or 0.5% bupivacaine provides a longer time for analgesia after Anterior Cruciate Ligament (ACL) reconstruction.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients scheduled for ACL reconstruction
  • ASA physical status I-II
  • Body weight > or = 50 kg.

Exclusion criteria

  • Patients with redo ACL reconstruction
  • Contraindication to neuraxial block
  • allergy to local anesthetics, sulfa, NSAIDs, morphine, paracetamol
  • Patients with communication problem

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

100 participants in 2 patient groups

0.25% bupivacaine
Active Comparator group
Description:
femoral nerve block using 0.25% bupivacaine versus 0.5% bupivacaine
Treatment:
Drug: 0.25% Bupivacaine
0.5% bupivacaine
Active Comparator group
Description:
femoral nerve block using 0.25% bupivacaine versus 0.5% bupivacaine
Treatment:
Drug: 0.5% Bupivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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