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.
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
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
Primary outcome measure(s)
Satisfaction level — 30 minutes per participant (including time to provide study information and complete the questionnaire) To evaluate patient satisfaction following a HyFoSy examination performed as part of an infertility workup by assessing the procedure's tolerability using a questionnaire administered immediately after the examination.
Participants will be asked to rate their overall satisfaction on a scale from 0 to 10, with 10 indicating the highest level of satisfaction.
Trial sites (1)
Facility
City
Region
Status
CHRU Nancy
Nancy
France
More Central Hospital, Nancy, France trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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