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NCT03087604 · ClinicalTrials.gov registry record · Phase 4

Loss of Resistance, w/wo Stimulation, For Epidural Placement

A Phase 4 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 4
Development phase
100
Enrollment target

NCT03087604 is a Phase 4 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 100 participants.

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The verdict

NCT03087604, a Phase 4 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 4
Development phase
100 participants
Enrollment target

Study Summary

The purpose of this randomized, observer-blinded, investigative trial is to determine if the use of electrical stimulation, compared to the traditional loss of resistance technique alone, improves the success rate of epidural catheter placement at an academic teaching institution.

Interventions

  • PROCEDURE Thoracic epidural block
  • PROCEDURE Electrical Nerve stimulation
  • DRUG Solution For Thoracic epidural block

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2017-03-17
Est. Completion 2017-10-11
Phase Phase 4

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT03087604

The ClinicalTrials.gov registry entry for NCT03087604 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Thoracic epidural block is the first listed.

NCT03087604 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03087604 about?

NCT03087604 is a clinical study titled "Loss of Resistance, w/wo Stimulation, For Epidural Placement". The purpose of this randomized, observer-blinded, investigative trial is to determine if the use of electrical stimulation, compared to the traditional loss of resistance technique alone, improves the success rate of epidural catheter placement at an academic teaching institution.

What is the current status of trial NCT03087604?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2017-03-17. Estimated completion is 2017-10-11.

What interventions are being tested in trial NCT03087604?

The interventions under investigation include: Thoracic epidural block (PROCEDURE), Electrical Nerve stimulation (PROCEDURE), Solution For Thoracic epidural block (DRUG).

Who is sponsoring clinical trial NCT03087604?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.