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Foam ultrasound for fertility checks: will women find it comfortable?

NCT ID NCT07736859

Symptom relief Sponsor: Central Hospital, Nancy, France 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time

Summary

This study asks women undergoing a HyFoSy (hysterosalpingo-foam sonography) exam as part of an infertility workup to rate their satisfaction and the procedure's tolerability. Participants fill out a questionnaire right after the exam, scoring their overall experience on a 0–10 scale. The goal is to see how well this foam-based ultrasound test is accepted by patients.

What this could mean

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

Active substance
Hysterosalpingo-foam sonography (HyFoSy) — an ultrasound procedure using foam to check the fallopian tubes
What this could lead to
If patients find HyFoSy highly tolerable, it could become a preferred first-step test for checking fallopian tube patency in fertility evaluations.
What could go wrong
This is a single-center observational study with no comparison group, so results may not apply to all clinics or patients. Satisfaction is subjective and may not reflect the procedure's diagnostic accuracy.

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.

Participants

About 200 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Sep 2027

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.

Who is studied

Women attending the fertility medicine unit who underwent a HyFoSy ultrasound examination.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 : * Provided verbal informed consent after receiving full information about the study procedures * Women * Aged 18 years or older * Attending the fertility medicine unit and undergoing a HyFoSy ultrasound examination * Affiliated with, or covered by, a social security health insurance scheme Exclusion Criteria : * Pregnant women * Women who are breastfeeding or in the postpartum period * Non-emancipated minors * Adults under legal protection (guardianship, curatorship, or judicial protection) * Adults unable to provide informed consent * Individuals deprived of liberty by judicial or administrative decision * Individuals receiving involuntary psychiatric care * Individuals who have declined participation in the study

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Conditions

The condition(s) this trial relates to.

infertility disorder Personal Satisfaction

As listed by the trial registrant

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

Infertility

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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

  • CHRU Nancy

    Nancy, 54000, France

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