Influence of Lumbar Ultrasound on Resident Learning Curve for Lateral Labor Epidural Placement

September 27, 2024 updated by: Michaela Kristina Farber, MD, Brigham and Women's Hospital

Pre-insertion Ultrasound Guidance for Labor Epidural Placement in the Lateral Position: A Randomized Controlled Trial of Image Reproducibility During Labor and Impact on Resident Learning Curve

The aim of this study is to evaluate the impact of lumbar spine ultrasound on the success rate and efficiency of labor epidural placement in the lateral position. The investigators hypothesize that ultrasound imaging of the lumbar spine of women in early labor will yield similar ultrasound results when done immediately prior to epidural placement. The investigators also hypothesize that the use of ultrasound with landmarks marked and depth to the epidural space estimated will facilitate epidural placement in terms of both efficiency (time required for placement) and efficacy of pain relief.

Study Overview

Status

Terminated

Intervention / Treatment

Detailed Description

Several studies have demonstrated a significant benefit in pre-procedural ultrasound for epidural placement by anesthesia residents, particularly when performed in the obese population. To the investigators knowledge, however, no studies have evaluated this teaching modality for the lumber epidural technique in the lateral position. Formalizing the educational process for this less frequently performed, highly technical and critical skill may have a profound impact on trainee learning curves, and may enhance the overall success and efficiency of epidural placement, quality of analgesia provided, and safety of the procedure.

Study Type

Interventional

Enrollment (Actual)

28

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Boston, Massachusetts, United States, 02115
        • Brigham and Women's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Pregnant Subjects

Inclusion Criteria:

  • pregnant women
  • 18 years or older
  • in early labor (cervix dilated < 5 cm
  • pain visual analog score (VAS) < 3, or both) requesting consultation by the anesthesia team for anticipated epidural pain relief.

Exclusion Criteria:

  • absolute contraindications of neuraxial anesthesia including patient refusal
  • uncorrected coagulopathy
  • infection at the skin site of epidural placement
  • increased intracranial pressure, or untreated hemodynamic instability.
  • In addition, patients with a history of scoliosis or spine surgery
  • body mass index (BMI) >40 kg/m2
  • allergy to local anesthetic, or allergy to opioids will be excluded.

Anesthesiologists

Inclusion criteria:

  • Anesthesia residents or fellows who are performing the epidural technique in pregnant subjects who agree to be part of the study.
  • Anesthesia residents or fellows with prior experience in the lumbar epidural technique, defined as having placed 20 or greater lumbar epidurals during their residency and prior to enrollment.

Exclusion criteria:

  • individuals who do not want to participate in the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Baseline ultrasound only, with no markings placed. No ultrasound prior to epidural placement.
Experimental: Ultrasound
Baseline and pre-puncture ultrasound with markings placed.
A baseline lumbar ultrasound in a standardized lateral position (by bed markings) will be performed with the midline and L3-L4 interspace marked, and estimated depth to the epidural space recorded. A second lateral lumbar ultrasound will be performed immediately prior to placement at the time of epidural request. The bed position will be standardized with lines drawn down the back, at the flexion of the knee, and heel of the foot. The sonographic measurements will include the midline, the L3-4 interspace, (both marked at the skin surface), and the measured depth to the ligamentum flavum (in centimeters).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Depth to the epidural space (cm) from baseline ultrasound compared to pre-placement ultrasound.
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Measured depth to the epidural space (cm) from baseline ultrasound compared to pre-placement ultrasound, measured with a 2-5 MHz curvilinear ultrasound probe at the lumbar spine, midline, at level L3-4.
From enrollment to time of epidural placement, approximately 5 hours
Time required for epidural placement
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Time required for placement (T0 = insertion of needle for subcutaneous lidocaine infusion prior to epidural needle placement). Tfinal = time at complete removal of Weiss epidural needle after catheter is threaded into the epidural space.
From enrollment to time of epidural placement, approximately 5 hours
Need for assistance from additional anesthesiologist
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Need for assistance from additional anesthesiologist
From enrollment to time of epidural placement, approximately 5 hours
Number of attempts at epidural placement
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
defined as number of times the Weiss epidural needle enters the skin
From enrollment to time of epidural placement, approximately 5 hours
Incidence of paresthesias
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Paresthesia defined as pain with needle or catheter insertion
From enrollment to time of epidural placement, approximately 5 hours
Labor pain at time of 30 minutes after placement is complete.
Time Frame: From enrollment to time of epidural placement, approximately 5 hours, plus 30 minutes.
Labor pain rated on a visual analog scale (VAS)
From enrollment to time of epidural placement, approximately 5 hours, plus 30 minutes.
Rate of epidural replacement for inadequate analgesia
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Inadequate analgesia determined as VAS >3 despite catheter adjustment and/or epidural dose adjustment.
From enrollment to time of epidural placement, approximately 5 hours
Rate of inadvertent dural puncture at the time of placement.
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Defined as cerebrospinal fluid aspiration through needle or catheter.
From enrollment to time of epidural placement, approximately 5 hours
Midline measurement from baseline ultrasound compared to pre-placement ultrasound.
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Measured midline (anatomical marking) from baseline ultrasound compared to pre-placement ultrasound, measured with a 2-5 MHz curvilinear ultrasound probe at the lumbar spine, midline.
From enrollment to time of epidural placement, approximately 5 hours
L3-L4 lumbar spine level measured from baseline ultrasound compared to pre-placement ultrasound.
Time Frame: From enrollment to time of epidural placement, approximately 5 hours
Measured L3-L4 lumbar spine level from baseline ultrasound compared to pre-placement ultrasound, measured with a 2-5 MHz curvilinear ultrasound probe at the lumbar spine, paramedic.
From enrollment to time of epidural placement, approximately 5 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Michaela K Farber, MD MS, Brigham and Women's Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2014

Primary Completion (Actual)

March 1, 2021

Study Completion (Actual)

March 1, 2021

Study Registration Dates

First Submitted

June 26, 2016

First Submitted That Met QC Criteria

July 7, 2016

First Posted (Estimated)

July 11, 2016

Study Record Updates

Last Update Posted (Actual)

October 1, 2024

Last Update Submitted That Met QC Criteria

September 27, 2024

Last Verified

September 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2013P002510

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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