Satisfaction of Hysterosalpingo-Foam Sonography

Enrolling by invitation

Conditions studied: Infertility

In brief

To evaluate patient satisfaction following a HyFoSy examination performed as part of a fertility workup, by assessing the procedure's tolerability through a questionnaire administered immediately after the examination.

Key facts

Study ID

NCT07736859

Run by

Central Hospital, Nancy, France

People needed

200

Starts

2026-09-01

Expected to finish

2027-09-01

Last updated by the study team

2026-07-30

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• CHRU Nancy — Nancy, France

Full record on ClinicalTrials.gov

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