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NCT03112642 · ClinicalTrials.gov registry record · NA

Nerve Stimulator for Patients With Upper Extremity Disease, Vascular or Orthopedic Surgery

A NA study, sponsored by Rutgers, The State University of New Jersey.

Terminated
Registry status
NA
Development phase
8
Enrollment target

NCT03112642: Clinical Trial NA study, sponsored by Rutgers, The State University of New Jersey.

NCT03112642 is a NA study that was terminated before completion, run by Rutgers, The State University of New Jersey. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03112642, a NA study, was terminated before completion, sponsored by Rutgers, The State University of New Jersey.

TERMINATED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

To help determine if there is improved pain relief when a device that makes an arm muscle move (nerve stimulator) is used to place a needle in the area above the collarbone to prevent feeling of pain (anesthesia) of the upper arm.

Primary Outcome

dermatomes (with full motor block) will be the outcome measure The investigators will be assessing changes between muscle strength in the myotomal distribution of the upper limb corresponding to the dermatome region of the brachial plexus following supraclavicular block, using the MRC power scale (medical research council scale, 0-5), with strength values obtained at time zero (initiation of the block), and to compared to subsequent measurements in 5 minute intervals until the final measurement

Interventions

  • PROCEDURE Local anesthetic block [0.35% marcaine]
  • DEVICE Braun DIG-R-C Stimuplex Blockade Monitor System

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2013-11
Est. Completion 2021-03-09
Phase NA

Why NCT03112642 stopped before completion

NCT03112642 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Local anesthetic block [0.35% marcaine] is the first listed.

NCT03112642 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03112642 about?

NCT03112642 is a clinical study titled "Nerve Stimulator for Patients With Upper Extremity Disease, Vascular or Orthopedic Surgery". To help determine if there is improved pain relief when a device that makes an arm muscle move (nerve stimulator) is used to place a needle in the area above the collarbone to prevent feeling of pain (anesthesia) of the upper arm.

What is the current status of trial NCT03112642?

This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2013-11. Estimated completion is 2021-03-09.

What interventions are being tested in trial NCT03112642?

The interventions under investigation include: Local anesthetic block [0.35% marcaine] (PROCEDURE), Braun DIG-R-C Stimuplex Blockade Monitor System (DEVICE).

Who is sponsoring clinical trial NCT03112642?

This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03112642's enrollment target sits among peer trials

8 1976th of 2000 higher than 19 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

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Source: ClinicalTrials.gov NCT03112642, the US trial registry maintained by the National Library of Medicine. NCT03112642 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.