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Analgesic Efficacy of Saphenous Nerve Blockade for Outpatient Knee Anterior Cruciate Ligament Surgery

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Status

Unknown

Conditions

Postoperative Analgesia for Anterior Cruciate Ligament Surgery of the Knee

Treatments

Procedure: Saphenous nerve blockade
Procedure: Femoral nerve blockade

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to determine whether blockade of the saphenous nerve can provide the same degree of analgesia postoperatively for ACLS as a femoral nerve block without resulting motor blockade enhancing shortening of hospital stay en functional outcome.

Enrollment

58 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 18-65 years
  • ASA status I - III
  • rupture of the anterior cruciate ligament.

Exclusion criteria

  • contraindication for regional anesthesia
  • allergy against local anesthetics
  • BMI > 35
  • pre-existing diagnosed neuropathy of the operated leg
  • ingestion of strong opioids
  • pregnancy or breastfeeding status
  • History of significant cardiovascular disease (MI, CVA, peripheral vascular disease)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

58 participants in 2 patient groups

Saphenous nerve blockade
Experimental group
Description:
Experimental treatment 15 mL of levobupivacaine 0.5%
Treatment:
Procedure: Saphenous nerve blockade
Femoral nerve blockade
Active Comparator group
Description:
Standard treatment 15 mL of levobupivacaine 0.5%
Treatment:
Procedure: Femoral nerve blockade

Trial contacts and locations

1

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Central trial contact

M.W. Hollmann, professor dr., MD; Werner ten Hoope, MD

Data sourced from clinicaltrials.gov

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