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New Tampon-Like device tested for Post-Sex comfort and safety

NCT ID NCT07445958

Symptom relief Sponsor: Atlantic Health System Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether using the Livi postcoital tampon three times in a row is safe for the vagina. Sixty sexually active women inserted and removed the device during one clinic visit. Doctors checked for any tissue damage or pain. The goal was to see if the device causes harm, not to compare it with other products.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Livi Postcoital Tampon Device (polyurethane foam pledget)
What this could lead to
If proven safe, this device could offer a comfortable way to manage postcoital discharge.
What could go wrong
This is a small, early safety study with no comparison group, so it cannot prove effectiveness or long-term safety.

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

60 people

The number who actually took part.

Started

Jan 2026

Finished

Feb 2026

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

18 years and older

Sex

Female participants only

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: * Sexually active women aged ≥18 years * Able and willing to comply with all study procedures * Able to provide written informed consent Exclusion Criteria: * Current pregnancy or within 6 weeks postpartum * Symptomatic vaginal infection, lesion, or vulvovaginal discomfort at baseline * Known allergy to any component of the study device * Pelvic or vaginal surgery within the past 6 weeks * Any medical or psychological condition that, in the investigator's opinion, may interfere with participation or safety

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Conditions

The condition(s) this trial relates to.

Coitus vaginal discharge

As listed by the trial registrant

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

Postcoital vaginal changes Vaginal discharge

Contacts and locations

Locations

  • Garden State Urology

    Mountain Lakes, New Jersey, 07046, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.