Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Ultrasound-guided transgluteal nerve block versus usual ER care for acute sciatica

Official title: Comparing Ultrasound-Guided Transgluteal Nerve Block to Standard Care for Emergency Department Patients With Low Back Pain and Sciatic Radiculopathy: A Randomized Controlled Trial

Run by University of California, San Francisco · NCT07397117 · Data updated 2026-11-12

This test tries a transgluteal sciatic nerve block to see if it reduces pain better than usual emergency-room care for adults with acute sciatica.

More Sciatica trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Locations1 site (San Francisco, California)
StatusRecruiting
StartedMay 26, 2026
Main results expectedDecember 31, 2026
Study endsJanuary 31, 2027
Registry record updatedJune 2, 2026
Trial IDNCT07397117 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older who present to the ED with unilateral sciatica-type lumbosacral radicular pain radiating to the leg and a pain score of at least 5/10, who can give informed consent and have no contraindications to nerve block, are ideal candidates.

Probably not a fit

Patients with neurological deficits (bowel/bladder dysfunction or leg weakness), suspected spinal infection or tumor, allergy to local anesthetics, active coagulopathy or anticoagulation, or inability to consent are excluded and unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults presenting to the emergency department with unilateral lumbosacral radicular pain and a pain score of 5/10 or higher will be randomized to receive either an ultrasound-guided transgluteal sciatic nerve block with ropivacaine or standard medical treatment. Pain scores and a short timed walking test will be recorded to compare short-term pain relief and functional improvement. Randomization and follow-up occur during the ED encounter and the immediate post-treatment period. The trial focuses on short-term outcomes in patients without neurologic deficits or contraindications to local anesthetic.

Why it matters

Potential benefit: If successful, this approach could provide faster and greater pain relief in the emergency department and reduce the need for systemic opioids while improving short-term mobility.

How similar studies have gone: Previous studies of peripheral nerve blocks for radicular and sciatic pain have shown short-term pain relief, but the specific transgluteal sciatic nerve block in ED patients has been less extensively studied.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18 years and older
* Presentation to ED with:
* Acute or acute-on-chronic pain consistent with sciatica, defined as unilateral lumbosacral radicular pain radiating from the lower back or gluteal region to the posterior leg, may extend distal to the knee.
* Pain score ≥ 5/10 on Numeric Rating Scale (NRS)

Exclusion Criteria:

* Known allergy to study medications (e.g., local anesthetics)
* Coagulopathy or current anticoagulation therapy
* Suspected or confirmed spinal infection, or tumor
* Neurological deficits (bowel or bladder dysfunction, leg weakness)
* Inability to provide informed consent

Where it's running

  • University of California, San Francisco
    San Francisco, California, United States
    Recruiting

Study contacts

  • Principal investigator: Jeanne Noble, MD — University of California, San Francisco
  • Study coordinator: Tianyu Tang, MD
  • Email: tianyu.tang@ucsf.edu
  • Phone: 628-247-7578

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.