Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04020042 · ClinicalTrials.gov registry record · NA

Epidural Placement Using Handheld Ultrasound Device vs. Traditional Landmark Palpation

A NA study, sponsored by University of Texas Southwestern Medical Center.

Terminated
Registry status
NA
Development phase
74
Enrollment target

NCT04020042: Clinical Trial NA study, sponsored by University of Texas Southwestern Medical Center.

NCT04020042 is a NA study that was terminated before completion, run by University of Texas Southwestern Medical Center. The registered enrollment target is 74 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04020042, a NA study, was terminated before completion, sponsored by University of Texas Southwestern Medical Center.

TERMINATED
Registry status
NA
Development phase
74 participants
Enrollment target

Study Summary

Ultrasound is widely in uses for vascular, nerve block and sometimes neuraxial block. The purpose of the study is to evaluate the impact of a handheld ultrasound device on the time to complete labor epidural placement and success rate of epidural analgesia in parturients with a wide range of body mass indexes (BMIs). A handheld ultrasound device (Accuro, Rhivanna Medical, Charlottesville, VA) may eliminate the time for equipment setup due to its portability and instant power-up. In addition, it provides a simulated diagram to aid in identifying bone and lumbar spaces. These unique features may be helpful in laboring women with a particular BMI range. We aim to define the usefulness of guidance with a handheld ultrasound in completing labor epidural analgesia in various BMIs. The primary outcome: The time needed to complete epidural placements. Secondary outcomes: * The number of needle insertion attempts, * The rate of success measured by the need to replacements during the labor course for vaginal or cesarean delivery.

Primary Outcome

The number of removal and insertion of the epidural needle until feeling epidural space.

Interventions

  • OTHER Ultrasound image guidance
  • OTHER Landmark palpation

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2019-08-28
Est. Completion 2021-03-23
Phase NA

Why NCT04020042 stopped before completion

NCT04020042 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Ultrasound image guidance is the first listed.

NCT04020042 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04020042 about?

NCT04020042 is a clinical study titled "Epidural Placement Using Handheld Ultrasound Device vs. Traditional Landmark Palpation". Ultrasound is widely in uses for vascular, nerve block and sometimes neuraxial block. The purpose of the study is to evaluate the impact of a handheld ultrasound device on the time to complete labor epidural placement and success rate of epidural analgesia in parturients with a wide range of body ma...

What is the current status of trial NCT04020042?

This trial is currently terminated. It is a NA study. The enrollment target is 74 participants. The study started on 2019-08-28. Estimated completion is 2021-03-23.

What interventions are being tested in trial NCT04020042?

The interventions under investigation include: Ultrasound image guidance (OTHER), Landmark palpation (OTHER).

Who is sponsoring clinical trial NCT04020042?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04020042's enrollment target sits among peer trials

74 1082nd of 2000 higher than 912 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03422731 · 74 participants · Early Phase 1

    Multi-modality Imaging and Collection of Biospecimen Samples in Understanding Bone Marrow Changes in Patients With Acute Myeloid Leukemia Undergoing TBI and Chemotherapy

  • NCT03804853 · 74 participants · NA

    Rehabilitation Following Reverse Total Shoulder Arthroplasty

  • NCT04065776 · 74 participants · NA

    Evaluation of Hippocampal-Avoidance Using Proton Therapy in Low-Grade Glioma

  • NCT04771156 · 74 participants · Phase 4

    Ketorolac in Palatoplasty

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04020042, the US trial registry maintained by the National Library of Medicine. NCT04020042 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.