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NCT06987201 · ClinicalTrials.gov registry record · NA

Effects of DigiVibe on Pain in Subjects Undergoing Intramuscular Injections, Subcutaneous Injections, and Fingersticks

A NA study, sponsored by East Coast Institute for Research.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT06987201 is a NA study that has completed, run by East Coast Institute for Research. The registered enrollment target is 20 participants.

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The verdict

NCT06987201, a NA study, has completed, sponsored by East Coast Institute for Research.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

This is a single-center, unblinded, prospective, cross-over study. The study population will include twenty (n=20) healthy subjects (10 men and 10 women) over the age of 18 with a self-reported fear/dislike of needles. Subjects who qualify for the study based on the study inclusion and exclusion criteria and who consent to participate in the study will undergo two (2) intramuscular (IM) injections in the deltoid muscle, two (2) subcutaneous (SC) injections in the abdomen, and two (2) fingersticks with a lancing device in the middle finger. One injection in each location will be performed using with no intervention (as per standard of care) and the other injection in each location will be performed using the DigiVibe device.

Interventions

  • DEVICE DigiVibe Vibration Anesthesia

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-08-04
Est. Completion 2025-08-15
Phase NA

What the Registry Record Tells You About NCT06987201

The ClinicalTrials.gov registry entry for NCT06987201 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is East Coast Institute for Research, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which DigiVibe Vibration Anesthesia is the first listed.

NCT06987201 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06987201 about?

NCT06987201 is a clinical study titled "Effects of DigiVibe on Pain in Subjects Undergoing Intramuscular Injections, Subcutaneous Injections, and Fingersticks". This is a single-center, unblinded, prospective, cross-over study. The study population will include twenty (n=20) healthy subjects (10 men and 10 women) over the age of 18 with a self-reported fear/dislike of needles. Subjects who qualify for the study based on the study inclusion and exclusion cri...

What is the current status of trial NCT06987201?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2025-08-04. Estimated completion is 2025-08-15.

What interventions are being tested in trial NCT06987201?

The interventions under investigation include: DigiVibe Vibration Anesthesia (DEVICE).

Who is sponsoring clinical trial NCT06987201?

This trial is sponsored by East Coast Institute for Research, which has 5 total clinical trials registered on ClinicalTrials.gov.

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

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.