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Genicular Nerve Block for Knee Pain in the ED

Ultrasound-Guided Genicular Nerve Block for Knee Pain in the Emergency Department: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07158736
Enrollment
34
Registered
2025-09-08
Start date
2025-08-06
Completion date
2026-09-01
Last updated
2026-02-12

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

Conditions

Knee Pain

Brief summary

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.

Interventions

genicular nerve block with ideal body-weight dosing of bupivacaine 0.5% with 4 mg dexamethasone

OTHERStandard of Care

This involves standard of care pain relief for patients who do not receive the genicular nerve block for knee pain, such as acetaminophen, non-steroidal anti-inflammatory drugs (NSAIDs), and opioids.

Sponsors

University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain level1 hour post-enrollmentMeasured by numeric rating scale: 0 (minimum value) - 10 (maximum value)

Secondary

MeasureTime frameDescription
Difference in Duration of Analgesia24 hoursPatients will be called back to assess their pain levels
Difference in AP-POQ-RED score1 hour after enrollment9 question survey study, all questions rated on 0 (minimum) - 10 (maximum) scale. Questions include: pain before and after treatment, pain with activities in and out of bed, emotions (anxiety, fear, helplessness), degree of pain relief in the emergency department, satisfaction.
Difference in length of stay in the emergency departmentAverage 1 hourLength of stay in the emergency department is determined from the time the provider first sees the patient to the time the provider discharges the patient.

Countries

United States

Contacts

CONTACTUmar Clinical Research Coordinator, AB
umar.aulia@pennmedicine.upenn.edu267-624-4394
PRINCIPAL_INVESTIGATORMichael M Shalaby, MD

University of Pennsylvania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026