NCT06245460

Brief Summary

Adductor canal block is an effective analgesic technique for major knee surgery. However, the saphenous nerve block is not sufficient to explain this block's efficiency. It has been shown that adductor canal block can spread to the tibial and fibular nerves through the adductor hiatus. However this diffusion's frequency has never been measured. The main objective of this study is to assess the frequency of the spread of the adductor canal block to the fibular and tibial nerves assessed by ultrasound observation at the popliteal fossa.

Trial Health

57
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2024

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 30, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 7, 2024

Completed
27 days until next milestone

Study Start

First participant enrolled

March 5, 2024

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 8, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 8, 2025

Completed
Last Updated

November 24, 2025

Status Verified

November 1, 2025

Enrollment Period

1.1 years

First QC Date

January 30, 2024

Last Update Submit

November 19, 2025

Conditions

Keywords

knee surgeryultrasoundanalgesiapain

Outcome Measures

Primary Outcomes (1)

  • Frequency of local anesthetic's spread

    The primary outcome is the frequency of local anesthetic's spread to tibial and fibular nerve during an adductor canal block, assessed by ultrasound imaging at the popliteal fossa level. The ultrasound images will be recorded and then assessed by two independent anesthesiologists.

    at baseline

Secondary Outcomes (2)

  • Frequency of altered sensibility

    at one and four hours

  • Correlation between local anesthetic spread and clinical alteration

    at baseline, hour 1 and hour 4th

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population will be all the consecutive patients scheduled for elective knee surgery under general anesthesia in our center and receiving an adductor canal block.

You may qualify if:

  • patients scheduled for elective knee surgery under general anesthesia
  • in center of Ambroise Paré hospital
  • receiving an adductor canal block

You may not qualify if:

  • patients cognitively impaired
  • patients suffering from peripheral neuropathy at the lower limb
  • patients receiving an IPACK block or surgical knee infiltration to complete the adductor canal block analgesia
  • patients who refused to take part in this study
  • pregnant or breastfeeding patients
  • patients under guardianship
  • imprisoned patients
  • patients without any medical insurance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of anesthesia, Ambroise Paré Hospital - APHP

Boulogne-Billancourt, 92100, France

Location

MeSH Terms

Conditions

Knee InjuriesAgnosiaPain

Condition Hierarchy (Ancestors)

Leg InjuriesWounds and InjuriesPerceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Romuald Henry, MD

    Department of anesthesia, Ambroise Paré Hospital - APHP

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 30, 2024

First Posted

February 7, 2024

Study Start

March 5, 2024

Primary Completion

April 8, 2025

Study Completion

April 8, 2025

Last Updated

November 24, 2025

Record last verified: 2025-11

Locations