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Genicular Nerve Block for Knee Pain in the ED

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University of Pennsylvania

Status

Enrolling

Conditions

Knee Pain

Treatments

Other: Standard of Care
Procedure: Genicular nerve block with bupivacaine and corticosteroids

Study type

Interventional

Funder types

Other

Identifiers

NCT07158736
IRB Protocol #858259

Details and patient eligibility

About

Patient with atraumatic knee pain without a large knee effusion on x-ray will be randomized to receive either a genicular nerve block (GNB) or standard of care in the emergency department.

Enrollment

34 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Atraumatic knee pain
  • >17 years age
  • X-ray of the knee obtained in the ED
  • Initial pain score (numeric rating scale) 5-10

Exclusion criteria

  • Fracture or dislocation on x-ray
  • large knee joint effusion identified on x-ray
  • allergy or contraindication to local anesthetics
  • History of local anesthetic systemic toxicity after receiving local anesthetics
  • Pregnancy
  • Incarcerated
  • History of knee replacement of affected knee
  • Concern for septic joint
  • Overlying cellulitis
  • Hemodynamic instability
  • Altered mental status or inability to consent for procedure.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

34 participants in 2 patient groups

Genicular Nerve Block
Experimental group
Description:
This arm of patients (17 total) will receive the genicular nerve block for their knee pain.
Treatment:
Procedure: Genicular nerve block with bupivacaine and corticosteroids
Standard of Care
Active Comparator group
Description:
This arm of patients (17 total) will receive standard of care analgesia for their knee pain
Treatment:
Other: Standard of Care

Trial documents
2

Trial contacts and locations

4

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Central trial contact

Umar Clinical Research Coordinator, AB

Data sourced from clinicaltrials.gov

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