Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:14 AM
Ignite Modification Date:
2025-12-25 @ 12:14 AM
NCT ID:
NCT01690858
Eligibility Criteria:
Inclusion Criteria:
* Inclusion criteria for females with repeated fetal losses:
* Age\> 18
* Female affiliated to French health insurance (Social Security),
* Informed consent form signed
* Patient with history of at least three foetal losses without any cause found (chromosomal abnormalities, uterine malformations, endocrine disorders, etc.)
Exclusion criteria for females with repeated fetal losses :
* Patient not fulfilling inclusion criteria
* Age \> 40
* Female unable to understand benefits and risks of protocol
* Female with history of repeated foetal losses of infectious or endocrine origin.
Inclusion criteria for females without repeated fetal losses:
* Age\> 18
* Female affiliated to the French health insurance (Social Security)
* Informed consent form signed
* Female without history of repeated foetal losses
Exclusion criteria for females without repeated fetal losses:
* Patient not fulfilling inclusion criteria
* Female with age above 40
* Female unable to understand benefits and risks of protocol
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT01690858
Study Brief:
Protocol Section:
NCT01690858