Prevalence of HPV Transmission During Medically Assisted Procreation Procedures (AMPAMAVIR)
Primary Purpose
Human Papillomavirus (HPV), Medically Assisted Procreation (MAP), Infertility
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Systematic HPV DNA assay in semen and cervicovaginal scrape
Systematic HPV DNA cervicovaginal scrape
systematic HPV Status in newborns in case of pregnancy
Sponsored by

About this trial
This is an interventional screening trial for Human Papillomavirus (HPV) focused on measuring medically assisted procreation
Eligibility Criteria
Inclusion Criteria:
- Age over 18
- Age under 40 for women
- Signed informed consent by both members of the couple
- Medical indication of MAP by AI (artificial insemination), IVF(in vitro fertilization) or ICSI (intracytoplasmic sperm injection) method
- Well understanding of information letter
Exclusion Criteria:
- Age over 40 for women
- Informed consent form not signed by one or both partners
- Co-infection of one of the partners or both by HIV (human immunodeficiency virus) , HBV (hepatitis B virus) and/or HCV (hepatitis C virus)
- IVF by only frozen embryo transfer at the time of inclusion
- Severe oligospermia in male partner (<500 000 sperm cells)
Sites / Locations
- Hôpital Jean VERDIER
- CHU de BORDEAUX
- CHU de CLERMONT-FERRAND
- Hôpital BICHAT
- CHU de SAINT-ETIENNE
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Population of couples candidate for MAP program
Arm Description
MAP = medically assisted procreation
Outcomes
Primary Outcome Measures
Presence of HPV DNA on a swab sampled in the throat of newborns from one or two parents detected positive for HPV in semen and/or cervicovaginal scrape
Secondary Outcome Measures
Presence of HPV DNA in seminal fractions: seminal plasma, sperm cells dedicated to MAP
Quantitative et qualitative parameters of spermogram analysis: volume of the ejaculate, number, mobility and morphology of sperm cells according to WHO criteria)
Genotype of HPV
Presence of HPV DNA in ovocytes samples and in embryo culture media
Quantitative and qualitative parameters of MAP procedures: fertilization rate, number of ovocytes, number of embryos…
Full Information
NCT ID
NCT02524223
First Posted
August 13, 2015
Last Updated
September 21, 2018
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Ministry of Health, France
1. Study Identification
Unique Protocol Identification Number
NCT02524223
Brief Title
Prevalence of HPV Transmission During Medically Assisted Procreation Procedures
Acronym
AMPAMAVIR
Official Title
Prevalence of HPV Transmission During Medically Assisted Procreation Procedures
Study Type
Interventional
2. Study Status
Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
July 12, 2012 (Actual)
Primary Completion Date
February 22, 2016 (Actual)
Study Completion Date
February 22, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Ministry of Health, France
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Human PapillomaVirus (HPV) are ones of the main causal agents of sexually transmitted diseases. Numerous HPV genotypes such as 16, 18, 31 or 45 are considered to be at high risk of oncogenicity especially for the anal and cervical mucosa. At the present time, no recommendations exist on the risk related to HPV during Medically Assisted Procreation (MAP) procedures. The main objective of this prospective multicentric cohort study is to evaluate the prevalence of transmission of HPV via the semen during MAP program. Secondary objectives are to evaluate (1) the prevalence of HPV DNA in the sperm fractions of men enrolled in MAP, (2) the efficacy of spermatozoal pellet preparation procedures to eliminate HPV, (3) the correlation between HPV and male infertility and (4) the correlation between HPV and success rate of procreation. Results could contribute to revise guidelines of MAP procedures and HPV vaccination policy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Papillomavirus (HPV), Medically Assisted Procreation (MAP), Infertility
Keywords
medically assisted procreation
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
915 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Population of couples candidate for MAP program
Arm Type
Other
Arm Description
MAP = medically assisted procreation
Intervention Type
Other
Intervention Name(s)
Systematic HPV DNA assay in semen and cervicovaginal scrape
Intervention Description
Screening of HPV status at the genital level of males enrolled in MAP program.
Intervention Type
Other
Intervention Name(s)
Systematic HPV DNA cervicovaginal scrape
Intervention Description
Screening of HPV status at the genital level of females enrolled in MAP program.
Intervention Type
Other
Intervention Name(s)
systematic HPV Status in newborns in case of pregnancy
Primary Outcome Measure Information:
Title
Presence of HPV DNA on a swab sampled in the throat of newborns from one or two parents detected positive for HPV in semen and/or cervicovaginal scrape
Time Frame
at birth
Secondary Outcome Measure Information:
Title
Presence of HPV DNA in seminal fractions: seminal plasma, sperm cells dedicated to MAP
Time Frame
At the time of enrollment, during MAP procedures and at birth (in case of)
Title
Quantitative et qualitative parameters of spermogram analysis: volume of the ejaculate, number, mobility and morphology of sperm cells according to WHO criteria)
Time Frame
At the time of enrollment, during MAP procedures and at birth (in case of)
Title
Genotype of HPV
Time Frame
At the time of enrollment, during MAP procedures and at birth (in case of)
Title
Presence of HPV DNA in ovocytes samples and in embryo culture media
Time Frame
At the time of enrollment, during MAP procedures and at birth (in case of)
Title
Quantitative and qualitative parameters of MAP procedures: fertilization rate, number of ovocytes, number of embryos…
Time Frame
At the time of enrollment, during MAP procedures and at birth (in case of)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age over 18
Age under 40 for women
Signed informed consent by both members of the couple
Medical indication of MAP by AI (artificial insemination), IVF(in vitro fertilization) or ICSI (intracytoplasmic sperm injection) method
Well understanding of information letter
Exclusion Criteria:
Age over 40 for women
Informed consent form not signed by one or both partners
Co-infection of one of the partners or both by HIV (human immunodeficiency virus) , HBV (hepatitis B virus) and/or HCV (hepatitis C virus)
IVF by only frozen embryo transfer at the time of inclusion
Severe oligospermia in male partner (<500 000 sperm cells)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas BOURLET, MD PhD
Organizational Affiliation
Centre Hospitalier Universitaire de Saint Etienne
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Jean VERDIER
City
Bondy
ZIP/Postal Code
93140
Country
France
Facility Name
CHU de BORDEAUX
City
Bordeaux
ZIP/Postal Code
33000
Country
France
Facility Name
CHU de CLERMONT-FERRAND
City
Clermont-ferrand
ZIP/Postal Code
63000
Country
France
Facility Name
Hôpital BICHAT
City
Paris
ZIP/Postal Code
75018
Country
France
Facility Name
CHU de SAINT-ETIENNE
City
Saint-etienne
ZIP/Postal Code
42055
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Prevalence of HPV Transmission During Medically Assisted Procreation Procedures
We'll reach out to this number within 24 hrs