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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02419261 |
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Date of registration:
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02/04/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Assessment of Adductor Canal Blockade in Anterior Cruciate Ligament Surgery
ACB |
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Scientific title:
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Assessment of Sensory and Motor Blockade of the Adductor Canal Blockade Performed for Surgery of Arthroscopic Anterior Cruciate Ligament Repair |
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Date of first enrolment:
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October 2014 |
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Target sample size:
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40 |
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Recruitment status: |
Unknown status |
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URL:
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https://clinicaltrials.gov/show/NCT02419261 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Belgium
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Contacts
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Name:
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Jean-Pierre H Lecoq, MD PhD |
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Address:
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Telephone:
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003243667180 |
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Email:
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jplecoq@chu.ulg.ac.be |
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Affiliation:
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Name:
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Jean-Pierre H Lecoq, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Liege, University Hospital |
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Name:
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Jean-Pierre H Lecoq, MD PhD |
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Address:
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Telephone:
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003243667180 |
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Email:
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jplecoq@chu.ulg.ac.be |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients scheduled for anterior cruciate ligament repair
Exclusion Criteria:
- Refusal to study,
- coagulation disorder,
- infection at the puncture site,
- preexisting neuropathy,
- allergy to local anesthetics,
- renal or hepatocellular insufficiency,
- context of chronic pain,
- drugs abuse,
- pregnant patient
Age minimum:
18 Years
Age maximum:
70 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Surgery of Arthroscopic Anterior Cruciate Ligament Repair
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Intervention(s)
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Procedure: Arthroscopic surgical repair of the anterior cruciate ligament
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Drug: Analgesic nerve blockade (Ropivacaine)
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Primary Outcome(s)
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Cold sensitivity assessment (cold, very cold, no sensation)
[Time Frame: From 30 to 60 minutes after nerve blockade]
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Motor blockade assessment (dynamometer)
[Time Frame: From 30 to 60 minutes after nerve blockade]
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Secondary Outcome(s)
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Postoperative pain assessment (visual analgesic scale)
[Time Frame: At 2, 4, 6 postoperative hours]
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Secondary ID(s)
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Gauthier - Lecoq - Goffin
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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