Recruiting NCT07170137
Comparison of Uterine Distension in Hysterosonography Among Patients Monitored for Infertility
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Infertile Women Undergoing IVF or ICSI, Distension by Volumetric Analysis of the Uterus. Basic parameters: 18 years — 43 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Comparison of differences in distension by volumetric analysis of the uterus before and after distension between groups of infertile and apparently fertile women.
Primary outcome measures
- uterine distension [Time frame: 1 years]
Eligibility criteria
Inclusion criteria
- Patient age ≥ 18 and < 43 years old
- No contraindications to pregnancy
- Patients consulting at the Saint Denis assisted reproductive technology (ART) department due to desire to become pregnant or infertility
Exclusion criteria
- Contraindication to assisted reproductive technology treatment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- Centre hospitalier Delafontaine — Saint-Denis
Identifiers
NCT: NCT07170137 · 0112.1_PMA