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NCT06034340 · ClinicalTrials.gov registry record · NA

Lidocaine Administration Using STAR Particles

A NA study, sponsored by Emory University.

Completed
Registry status
NA
Development phase
22
Enrollment target

NCT06034340: Completed NA study, sponsored by Emory University.

NCT06034340 is a NA study that has completed, run by Emory University. The registered enrollment target is 22 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06034340, a NA study, has completed, sponsored by Emory University.

COMPLETED
Registry status
NA
Development phase
22 participants
Enrollment target

Study Summary

This study is being done to answer the question: Do STAR particles (tiny pieces of ceramic with small spikes) help numbing gel (a gel that helps you feel less pain) work more quickly to provide local anesthesia or numbing in a specific area? Research participants will provide feedback on how quickly the STAR particles with the numbing gel can provide anesthesia. Participants will report their sensation at either 10 or 20 minutes after application of the numbing gel.

Primary Outcome

The time to achieve anesthesia is assessed as the percent of sharp (as opposed to dull) sensation reported at 10 or 20 minutes after the application of LET gel.

Interventions

  • DEVICE LET Gel after STAR Particle Application (Right or Left Arm)
  • OTHER LET Gel Application without STAR Particle Application (Contralateral Arm)

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2023-03-19
Est. Completion 2023-06-13
Phase NA
Emory University

1,208 total trials

What the finished NCT06034340 record still lists

NCT06034340 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which LET Gel after STAR Particle Application (Right or Left Arm) is the first listed.

NCT06034340 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06034340 about?

NCT06034340 is a clinical study titled "Lidocaine Administration Using STAR Particles". This study is being done to answer the question: Do STAR particles (tiny pieces of ceramic with small spikes) help numbing gel (a gel that helps you feel less pain) work more quickly to provide local anesthesia or numbing in a specific area? Research participants will provide feedback on how quickly...

What is the current status of trial NCT06034340?

This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2023-03-19. Estimated completion is 2023-06-13.

What interventions are being tested in trial NCT06034340?

The interventions under investigation include: LET Gel after STAR Particle Application (Right or Left Arm) (DEVICE), LET Gel Application without STAR Particle Application (Contralateral Arm) (OTHER).

Who is sponsoring clinical trial NCT06034340?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06034340's enrollment target sits among peer trials

22 1756th of 2000 higher than 239 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 NCT06034340, the US trial registry maintained by the National Library of Medicine. NCT06034340 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.