ClinicalTrials.Veeva

Menu

Impact of Human Papillomavirus Carriage on IVF/ICSI Results (HPV AMP) (HPV-AMP)

R

Regional University Hospital Center (CHRU)

Status

Enrolling

Conditions

Human Papilloma Virus
Infertility, Female

Study type

Observational

Funder types

Other

Identifiers

NCT06550531
29BRC21.0363 - HPV AMP

Details and patient eligibility

About

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.

Full 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

Enrollment

618 estimated patients

Sex

Female

Ages

25 to 38 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

Loading...

Central trial contact

Anne-Solenn JACAMON; Sarah BOUEE

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems