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Evaluation by Ultrasound Imaging of Local Anesthetic Spread to the Popliteal Fossa During an Adductor Canal Block
EchoCAdd
2 other identifiers
observational
30
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Mar 2024
1 active site
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
CompletedFirst Posted
Study publicly available on registry
February 7, 2024
CompletedStudy Start
First participant enrolled
March 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 8, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 8, 2025
CompletedNovember 24, 2025
November 1, 2025
1.1 years
January 30, 2024
November 19, 2025
Conditions
Keywords
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
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
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Romuald Henry, MD
Department of anesthesia, Ambroise Paré Hospital - APHP
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