CompletedNot Applicable

Postoperative Analgesic Benefit of iPACK Block in the Anterior Cruciate Ligament Reconstruction Surgery

France90 participantsStarted 2021-12-13

Plain-language summary

This randomised clinical trial evaluates the analgesia provided by an iPack block associated with an adductor canal block in patients who undergo anterior cruciate ligament reconstruction surgery, compared to an adductor canal block alone. The objective is to prove the superiority of this locoregional anesthesia in terms of analgesia and functional rehabilitation.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age ≥ 18 years * ACL repair surgery under general anesthesia * Person affiliated or beneficiary of a social security plan * Free, informed and written consent Exclusion Criteria: * Age \< 18 years * Contraindication to ALR (allergy to local anesthetics, local infection of the puncture site, coagulopathy) * Pre-existing opiate dependence * Contraindication to non-steroidal anti-inflammatory drugs * Pregnant or potentially pregnant women * Patients under the protection of adults (guardianship, curatorship or safeguard of justice) * Patients whose cognitive state does not allow evaluation by the scales used

What they're measuring

Cumulative opioid consumption at 48 hours after surgery

Timeframe: Hours 48

Trial details

NCT IDNCT05136352

SponsorUniversity Hospital, Toulouse

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-06-30

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