CHRU de Brest
Brest, 29609, France
Location status: Recruiting
NCT Number: NCT06550531
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.
Interested in participating?
Request Info25 year–38 year
Female
Observational
Brest, 29609, France
Location status: Recruiting
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
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Age < 25 y Age > ou = 38 y AMH < 1.1 ng/ml patient under juridic protection rejection of participation
Time frame: 1 year
A clinical pregancy is the visualisation of a gestational sac inside the uterus after 6 weeks of gestation
Time frame: 1 year
oocytes number, embryos number, fecondation rate, implantation rate
Time frame: 1 year
number of women who have a positive HPV test before IVF procedure
Interested in participating?
Request InfoUniversity Hospital, Brest
Other
Impact of Human Papillomavirus Carriage on IVF/ICSI Results at Brest University Hospital
Acronym: HPV-AMP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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