WithdrawnNot Applicable

Knee Arthroscopy for Pain Control

Stopped: The study never started.

0Started 2025-12

Plain-language summary

This study aims to determine the effectiveness of an anterolateral genicular nerve block and portal anesthesia in controlling pain in the perioperative period after knee arthroscopy. Opioid consumption, the use of non-opioid medications, complication rate, and sleep quality will also be measured.

Who can participate

Age range19 Years – 89 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: * skeletally mature patients with indications for knee arthroscopy Exclusion Criteria: * include patients with previous knee surgery on the operative side * opioid use within six weeks before surgery that is deemed to be chronic or excessive * gabapentin use within six weeks before surgery * diagnosis of chronic pain, fibromyalgia, or other somatosensory disorder(s) * history of radicular pain or neuropathy in the operative limb * patients with cancer

What they're measuring

Postoperative Pain Management

Timeframe: 2, 4, 6, 12, 24, and 48 hours and 1 week post-op

Trial details

NCT IDNCT06701175

SponsorUniversity of Alabama at Birmingham

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-08

View on ClinicalTrials.gov More Knee Arthroscopy trials