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ACL-GAIN trial

Adductor Canal Block without versus with Anterolateral Genicular Nerve Block for Postoperative Pain Management after Anterior Cruciate Ligament Reconstruction with Anterolateral Corner Reconstruction: A Prospective Multicenter Randomized Controlled Trial - Adductor Canal Block with versus without Anterolateral Genicular Nerve Block for Pain after ACL and ALC Reconstruction: The ACL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58421
Enrollment
80
Registered
2025-10-09
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament tear, Anterolateral Corner Injury Ruptured Anterior Cruciate Ligament

Interventions

Anterolateral genicular nerve block using ropivacaine

Sponsors

Ziekenhuis Gelderse Vallei
Lead Sponsor

Eligibility

Age
16 Years to 64 Years

Inclusion criteria

Inclusion criteria: -Clinical indication and willingness to undergo combined ACL and anterolateral corner reconstruction-(Sub)total primary ACL tear on physical examination and MRI, with or without concomitant meniscal injury and/or cartilage injury and/or partial concomitant knee ligament injury not requiring surgery-Age 16 years and older -Preinjury Tegner score  5 and desire to return to preinjury level 

Exclusion criteria

Exclusion criteria: -Multiligamentous knee injury requiring multiligamentous knee surgery-Patients undergoing ACL revision surgery-Contraindications to peripheral nerve blocks including but not limited to local infection at the injection site, significant hematological disease, allergy to local anasthetics, and relevant cardiovascular conditions (e.g. atrioventricular conduction disorders, use of anti-arrhythmic medication)-Pre-existing neurological deficits-Pre-existing chronic pain condition not related to ACL injury-History of allergy to drugs used in this study-No understanding of Dutch language or not capable of understanding the study and participation-Pregnancy or breastfeeding at the time of surgery or during the perioperative study period

Design outcomes

Primary

MeasureTime frame
The primary outcome is the Numeric Rating Scale (NRS) pain score during movement at 2 hours postoperatively

Secondary

MeasureTime frame
Secondary outcomes include cumulative opioid consumption, use of rescue analgesics, patient-reported outcomes (VAS-pain, IKDC-subjective, Tegner, Lysholm, ACL-RSI) at six weeks, and incidence of adverse events. Statistical analyses include mixed-effects models to compare outcomes between groups while adjusting for baseline variables.

Countries

Netherlands

Contacts

Public ContactW.A. van der Wal

Ziekenhuis Gelderse Vallei

walw@zgv.nl+31318435247

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Mar 20, 2026