Ultrasound vs Palpation for Spinal Tap

Enrolling by invitation at 1 trial location
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: The Cooper Health System
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The goal of this randomized clinical trial is to determine whether ultrasound-assisted lumbar puncture improves first-needle insertion success compared with the standard palpation technique in adults undergoing a clinically indicated lumbar puncture.

The primary question is whether pre-procedural ultrasound localization increases the likelihood of successful cerebrospinal fluid collection on the first needle insertion. The study will also evaluate overall procedural success, the number of needle insertions and redirections, procedure time, the need for subsequent image-guided lumbar puncture, traumatic tap, procedural and post-procedural pain, and post-dural puncture headache.

Participants will be randomly assigned in a 1:1 ratio to undergo lumbar puncture using either pre-procedural ultrasound localization or standard palpation of anatomical landmarks.

Are You a Good Fit for This Trial?

This trial is for adults who need a lumbar puncture (spinal tap) as part of their medical care. People with certain conditions or reasons that make the procedure unsafe may not be able to join.

Inclusion Criteria

I am 18 years old or older.
I need a lumbar puncture as part of my treatment or diagnosis.
I can give consent or have someone legally authorized to do so for me.

Exclusion Criteria

I have an infection where the lumbar puncture would be done.
I received blood clot prevention medicine on the day of my lumbar puncture.
I cannot safely have a lumbar puncture, as decided by my doctor.
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What Are the Treatments Tested in This Trial?

Interventions

  • Standard Palpation-Guided Lumbar Puncture
  • Ultrasound-Assisted Lumbar Puncture

Trial Overview

The study compares two ways of doing a lumbar puncture: one uses ultrasound imaging to help guide needle placement, and the other relies on feeling anatomical landmarks by hand. Participants are randomly assigned to either method.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Ultrasound-assistedExperimental Treatment1 Intervention
Group II: Standard Palpation-GuidedActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

The Cooper Health System

Lead Sponsor

Trials
82
Recruited
35,600+