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Quadriceps Motor Unit Adaptation to Simulated Knee Injury

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University of Central Florida

Status

Not yet enrolling

Conditions

Muscle Inhibition
Knee Injury Simulation

Treatments

Drug: Intra-articular Lidocaine
Device: Joint Effusion via 60 mL Sterile Saline
Other: Sham injection

Study type

Interventional

Funder types

Other

Identifiers

NCT06999057
Knee_Injection_Study:6295

Details and patient eligibility

About

This study investigates how simulated knee injury-via artificial joint effusion or deafferentation-affects quadriceps motor unit behavior in healthy young adults. Participants will complete neuromuscular testing during a single 2-hour lab session. This research seeks to improve understanding of muscle inhibition and inform interventions after real-world knee trauma.

Full description

Using a controlled laboratory model, the investigators will simulate knee injury through two methods: (1) intra-articular saline injection to induce effusion, and (2) intra-articular lidocaine injection to induce sensory deafferentation. Healthy participants aged 18-30 will undergo surface and decomposition EMG, isometric strength testing, and reflex measurements before and after the intervention. The primary outcome is motor unit recruitment characteristics, with secondary outcomes including quadriceps inhibition (Hoffmann reflex) and isometric peak torque. The findings will inform future neuromodulatory approaches in rehabilitation.

Enrollment

45 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age 18-30 years
  2. Physically active (Tegner ≥ 5)
  3. No prior lower-limb surgery or major injury

Exclusion criteria

  1. Lower limb surgery or significant injury in past 2 years
  2. Cardiopulmonary, neurological, or psychiatric disorders
  3. Needle/electrical stimulation anxiety
  4. Medications affecting neuromuscular or psychological function
  5. Pregnancy
  6. Allergic to lidocaine
  7. Inability to elicit Hoffmann reflex

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

45 participants in 3 patient groups

Effusion Group
Experimental group
Description:
60 mL sterile saline injected into knee
Treatment:
Device: Joint Effusion via 60 mL Sterile Saline
Deafferentation Group
Active Comparator group
Description:
Lidocaine (single intra-articular dose)
Treatment:
Drug: Intra-articular Lidocaine
Control Group
Sham Comparator group
Description:
Sham procedure with fake needle
Treatment:
Other: Sham injection

Trial contacts and locations

0

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Central trial contact

Meredith Chaput, Ph.D.; Grant Norte, Ph.D.

Data sourced from clinicaltrials.gov

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