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NCT02464176 · ClinicalTrials.gov registry record · Phase 4

Systemic Steroids for Peripheral Nerve Blocks

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

Completed
Registry status
Phase 4
Development phase
115
Enrollment target

NCT02464176: Completed Phase 4 study, sponsored by Wake Forest University Health Sciences.

NCT02464176 is a Phase 4 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 115 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02464176, a Phase 4 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 4
Development phase
115 participants
Enrollment target

Study Summary

This study will investigate the ability of systemic dexamethasone to prolong the sensory block duration for lumbar plexus nerve blockade.

Primary Outcome

The primary outcome will be duration of sensory blockade in the distribution of the lumbar plexus as determined by pin-prick sensation as tested every two hours with pin-prick sensation.

Interventions

  • DRUG Bupivacaine
  • DRUG Dexamethasone
  • DRUG Epinephrine
  • DRUG Saline
  • PROCEDURE Lumbar Plexus Nerve Block

Trial Details

FieldValue
Enrollment Target 115 participants
Start Date 2015-06
Est. Completion 2017-01
Phase Phase 4
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT02464176 record still lists

NCT02464176 is an interventional study that assigns participants to a tested intervention. The registered 115 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (78% lower).

The record links to 0 conditions, and to 5 interventions - of which Bupivacaine is the first listed.

NCT02464176 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02464176 about?

NCT02464176 is a clinical study titled "Systemic Steroids for Peripheral Nerve Blocks". This study will investigate the ability of systemic dexamethasone to prolong the sensory block duration for lumbar plexus nerve blockade.

What is the current status of trial NCT02464176?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 115 participants. The study started on 2015-06. Estimated completion is 2017-01.

What interventions are being tested in trial NCT02464176?

The interventions under investigation include: Bupivacaine (DRUG), Dexamethasone (DRUG), Epinephrine (DRUG), Saline (DRUG), Lumbar Plexus Nerve Block (PROCEDURE).

Who is sponsoring clinical trial NCT02464176?

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

How this trial's enrollment target compares

Where NCT02464176's enrollment target sits among peer trials

115 718th of 2000 higher than 1,281 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT02464176, the US trial registry maintained by the National Library of Medicine. NCT02464176 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.