Actively Recruiting

Age: 18Years +
All Genders
NCT07221903

The Lateral, Anterior, Medial (LAM) Femoral Cutaneous Block: A Case Series Harborview Medical Center, Seattle, WA

Led by University of Washington · Updated on 2025-11-04

10

Participants Needed

1

Research Sites

62 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Skin donor sites in patients undergoing split-thickness skin grafting surgeries can be very painful postoperatively. This site is most often the anterolateral thigh, the pain at which location can traditionally be covered by a fascia iliaca nerve block, although that comes with the disadvantage of losing motor functions in the femoral nerve distribution. The LAM nerve block, which is relatively new, aims to provide analgesia in the distribution of the lateral and anterior femoral cutaneous nerves. In short, this nerve block would decrease the sensation of the anterolateral thigh area without affecting the motor function of the leg. Investigators aim to study the consistency and coverage size of sensation changes by mapping out the area after the block in each patient.

CONDITIONS

Official Title

The Lateral, Anterior, Medial (LAM) Femoral Cutaneous Block: A Case Series Harborview Medical Center, Seattle, WA

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Scheduled surgery for split-thickness skin graft with donor site from the thigh
  • Care team requests LAM nerve block
  • Expected postoperative pain in the anterior and lateral thigh skin areas
Not Eligible

You will not qualify if you...

  • Unable to communicate changes in sensation or movement
  • Existing sensory or motor problems in the femoral nerve area
  • Allergy to amide local anesthetics or severe liver dysfunction
  • Injection site infection or other contraindication to nerve block
  • Pregnant
  • Prisoner status
  • Does not read or speak English
  • Surgery lasting 6 hours or more
  • Total body surface area burn 20% or greater
  • Severe injuries like major bone fractures or polytrauma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Harborview Medical Center

Seattle, Washington, United States, 98104

Actively Recruiting

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Research Team

A

Adrienne James

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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