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Trial Title:
Impact of Human Papillomavirus Carriage on IVF/ICSI Results (HPV AMP)
NCT ID:
NCT06550531
Condition:
Human Papilloma Virus
Infertility, Female
Conditions: Official terms:
Papilloma
Infertility
Infertility, Female
Study type:
Observational
Overall status:
Recruiting
Study design:
Time perspective:
Prospective
Summary:
The prevalence of the papilloma virus in the general population is 12%. This virus is
known to impair male fertility but its impact on female infertility remains uncertain.
This is a public health problem since there is a vaccination protocol. Demonstrating the
impact of the human papillomavirus on fertility would be an argument in favor of
vaccination.
Detailed description:
This is a single-center prospective study in the assisted reproduction center of Brest
University Hospital. All new patients coming to consult will be offered participation in
the study. The HPV test will be updated if it is older than 12 months. We will analyze
stimulation results and pregnancy outcomes according to HPV status. Inclusions will take
place over 3 years
Criteria for eligibility:
Study pop:
The population study is a population of infertile women who are consulting in our center
of Reproduction Médicine in CHU Brest.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- all etiology of infertility AMH > ou = à 1.1 ng/ml First ou second protocol of IVF
between 25 years and 37 years and 11 months
Exclusion Criteria:
Age < 25 y Age > ou = 38 y AMH < 1.1 ng/ml patient under juridic protection rejection of
participation
Gender:
Female
Minimum age:
25 Years
Maximum age:
38 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
CHRU de Brest
Address:
City:
Brest
Zip:
29609
Country:
France
Status:
Recruiting
Contact:
Last name:
Sarah BOUEE
Email:
sarah.bouee@chu-brest.fr
Start date:
February 4, 2022
Completion date:
February 4, 2026
Lead sponsor:
Agency:
University Hospital, Brest
Agency class:
Other
Source:
University Hospital, Brest
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06550531
