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

NCT03090295 · ClinicalTrials.gov registry record · NA

Palpation and ACCURO for Placing Spinal in C-section

A NA study, sponsored by University of Virginia.

Completed
Registry status
NA
Development phase
80
Enrollment target

NCT03090295: Completed NA study, sponsored by University of Virginia.

NCT03090295 is a NA study that has completed, run by University of Virginia. The registered enrollment target is 80 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03090295, a NA study, has completed, sponsored by University of Virginia.

COMPLETED
Registry status
NA
Development phase
80 participants
Enrollment target

Study Summary

The Accuro is a three dimensional handheld ultrasound device. This device uses sound waves to create pictures of the spine in three dimensions. This may allow the physician to view the spine in more detail for procedures such as spinal anesthesia and other diagnostic procedures. We aim to assess the benefit of using both the Accuro and traditional landmark palpation technique to determine accurate spinal level in women who undergo cesarean section. This study will also assess provider preference for use of both Accuro and palpation compared with palpation alone or use of Accuro alone. Anesthesia Providers will first identify the L4/L5 space using the traditional technique of palpating the iliac crests to estimate spinal level, which will be marked with a single dot from a marking pen. The provider will then use the Accuro 3000 to identify the L4/L5 interspace. Results will be compared to results obtained in IRB 18070 "Handheld 3D lumbar spine navigation: A clinical validation study RM002" where subjects who were undergoing a C-section were randomized to either palpation or Accuro alone.

Primary Outcome

Success rates: defined as successful spinal administration on the first needle insertion attempt.

Interventions

  • DEVICE Palpation and Accuro

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2017-03-13
Est. Completion 2018-03-30
Phase NA
University of Virginia

449 total trials

What the finished NCT03090295 record still lists

NCT03090295 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which Palpation and Accuro is the first listed.

NCT03090295 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03090295 about?

NCT03090295 is a clinical study titled "Palpation and ACCURO for Placing Spinal in C-section". The Accuro is a three dimensional handheld ultrasound device. This device uses sound waves to create pictures of the spine in three dimensions. This may allow the physician to view the spine in more detail for procedures such as spinal anesthesia and other diagnostic procedures. We aim to assess th...

What is the current status of trial NCT03090295?

This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2017-03-13. Estimated completion is 2018-03-30.

What interventions are being tested in trial NCT03090295?

The interventions under investigation include: Palpation and Accuro (DEVICE).

Who is sponsoring clinical trial NCT03090295?

This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03090295's enrollment target sits among peer trials

80 994th of 2000 higher than 941 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

  • NCT01243931 · 80 participants · NA

    Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy

  • NCT01659203 · 80 participants · Phase 1

    Proton or Photon RT for Retroperitoneal Sarcomas

  • NCT01803451 · 80 participants · Early Phase 1

    Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass

  • NCT01964859 · 80 participants · Phase 2

    Feasibility Study for Fibroblast Autologous Skin Grafts

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 NCT03090295, the US trial registry maintained by the National Library of Medicine. NCT03090295 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.