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New tool aims to make baby shots less painful

NCT ID NCT06624176

Symptom relief Sponsor: Lauren Fortier Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a device called ShotBlocker can lower pain in healthy full-term newborns receiving their first Hepatitis B vaccine. Researchers will compare heart rate, oxygen levels, and pain scores between babies who get standard care (swaddling and sugar water) and those who also have ShotBlocker pressed against the injection site. 200 infants will take part to see if this simple tool adds extra comfort.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2024

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

37 to 42 weeks

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Infants born at UMass Memorial Medical Center (UMMMC) via vaginal delivery or cesarean delivery and under the care of the nursery team * Term infants (37 to 42 weeks gestational age) * No acute illness that causes pain * Apgar score above 7 at 5 minutes * Have successfully attempted at least one oral feeding * No circumcision in the last 6 hours * Parental consent for Hepatitis B vaccine Exclusion Criteria: * Swallow dysfunction * Congenital or genetic abnormalities * Infants who were exposed to sedatives within the last 12 hours * Infants with skin on thigh, hand, or foot that is not intact * Diagnosis of Neonatal Abstinence Syndrome (NAS) * Infants who are simultaneously receiving Hepatitis B Immunoglobulin or Nirsevimab (RSV vaccine) * Department of Children and Families (DCF) custody

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Conditions

The condition(s) this trial relates to.

Needlestick Injuries

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Neonatal pain

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • UMass Memorial Medical Center- Memorial Campus

    RECRUITING

    Worcester, Massachusetts, 01605, United States

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