Human Papilloma VirusNCT06161727
Detection and Prevalence of Human Papillomavirus (HPV) in Seminal Plasma and/or on Sperm in Men Undergoing Treatment With IVF/ICSI.
An observational study of Human Papilloma Virus and Infertility, Male, run by Vastra Gotaland Region at 1 site in Sweden.
Trial summary
This observational study aims to investigate the presence of HPV DNA in semen samples from men undergoing in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) treatment. It focuses on understanding the impact of HPV on male fertility and embryo development following IVF/ICSI. Read more about this study
- Who is it for?
- Ages 18 to 60 years, men only
- Conditions the study is for
- Human Papilloma Virus, Infertility, Male
- What is being tested?
- HPV exposure
- How many people
- 260 participants
- Where
- 1 siteSweden
- Study dates
- 1 Jan 2023to 28 Mar 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- Men only
- Adult
Study population: Men undergoing infertility treatment with IVF/ICSI and fresh ejaculated sperm at Sahlgrenska University Hospital (SU), Gothenburg, Sweden.
Who may be able to join
- Over the course of one year, the study will include men undergoing infertility treatment with IVF/ICSI and fresh ejaculated sperm at Sahlgrenska University Hospital (SU), Gothenburg, Sweden.
Who cannot join
- Men undergoing IVF/ICSI treatments with surgically extracted sperm.
- Men undergoing sperm freezing for fertility preservation purposes or possessing previously frozen sperm.
- Sperm donors.
- Men for whom treatment with preimplantation genetic testing (PGT) or egg donation is planned.
Trial locations and contacts
1 site in 1 country.
Sweden1 site
Department of Obstetrics and Gynecology, Sahlgrenska University Hospital
Gothenburg, 24
About this study
Official title: Detection and Prevalence of Human Papillomavirus (HPV) in Seminal Plasma and/or on Sperm in Men Undergoing Treatment With IVF/ICSI in Southwestern Sweden: a Prospective Study.
This observational study aims to investigate the presence of HPV DNA in semen samples from men undergoing in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) treatment. It focuses on understanding the impact of HPV on male fertility and embryo development following IVF/ICSI. The primary goal is to determine the prevalence of HPV-positive (HPV+) semen samples among men seeking infertility treatment with IVF/ICSI. Additionally, the study aims to compare semen characteristics between HPV-positive and HPV-negative (HPV-) samples and assess the embryological outcomes after IVF/ICSI in these two groups.
Participants in this study will include men receiving IVF/ICSI treatment and providing fresh ejaculated sperm at Sahlgrenska University Hospital in Gothenburg, Sweden, over one year. Those undergoing treatments with surgically extracted sperm, sperm freezing for fertility preservation, or planning treatments involving preimplantation genetic testing or egg donation will be excluded.
The study will involve analyzing HPV DNA in semen samples through PCR, utilizing the most effective method for HPV DNA detection previously identified in a pilot study. Sperm samples collected during infertility investigations and IVF/ICSI treatments will undergo gradient centrifugation to separate different components. A portion of the sperm sample will be preserved for PCR analysis to detect HPV DNA, while the rest will be used for IVF/ICSI procedures. The results from the PCR analyses will be correlated with semen characteristics and the outcomes of IVF/ICSI treatment. Furthermore, the samples will be stored for potential future analyses related to HPV-related biomarkers for up to 5 years at Biobank.
Read the detailed description
Infection with the human papillomavirus (HPV) represents one of the most widespread sexually transmitted diseases, affecting both genders. Over 100 types of HPV can cause infections in the skin or mucous membranes and are typically transmitted through skin-to-skin contact, vaginal or anal intercourse, as well as oral sex. Statistics indicate that between 50 and 80 percent of sexually active adults will experience genital HPV infections during their lifetime. These infections tend to be persistent, especially in men. Although most HPV infections are asymptomatic, they can lead to genital warts, dysplasia, cancer, infertility, and may impact the outcomes of in vitro fertilization (IVF). Despite extensive research on HPV-related conditions in women, there has been limited attention given to HPV-related conditions in men.
A systematic review and meta-analysis conducted in 2017, comprising 31 studies, revealed that the prevalence of HPV DNA in semen samples among men in the general population was 11.4%, rising to 20.4% among men with infertility. It remains unclear whether HPV localizes in seminal plasma or in cellular fractions of semen samples (such as sperm, epithelial cells, or leukocytes). Recent evidence has shown that HPV DNA can be found on the surface of sperm by binding to specific glycosaminoglycans (GAGs), such as syndecan-1, along the equatorial region of the sperm head. Additionally, a few in vitro studies have indicated that HPV DNA can be found inside sperm when mixed with the HPV virus. The potential effects of HPV on fertility are not yet fully understood. The presence of HPV infection in sperm has been associated with impaired sperm parameters, mainly sperm motility, and increased sperm DNA fragmentation. Existing evidence suggests a negative effect of HPV DNA in seminal plasma and/or on sperm on the number of live births and ongoing pregnancies, although the level of evidence remains limited. Considering that sperm is utilized in IVF, it is crucial to investigate the presence of HPV in seminal plasma and sperm in these men, as well as any potential consequences on embryo development following IVF.
The primary objective of this study is to assess the prevalence of HPV DNA in seminal plasma and/or on sperm in men undergoing in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) treatments. Furthermore, the study aims to characterize semen parameters in men with HPV-positive (HPV+) and HPV-negative (HPV-) semen samples and analyze the embryological outcomes after IVF/ICSI in men with HPV+ semen samples compared to men with HPV- semen samples.
The secondary objectives include evaluating semen parameters such as volume, sperm concentration, and motility to determine if there are differences between men with HPV+ and HPV- semen samples. Additionally, the study aims to investigate whether the embryological outcome (fertilization rate, number of high-quality embryos) after IVF/ICSI treatment differs between men with HPV+ and HPV- semen samples.
Analyses of HPV DNA in seminal plasma and/or on sperm will be conducted using the method that has demonstrated the highest performance in detecting HPV DNA, based on a previously conducted pilot study. Sperm samples are typically provided at the Fertility Laboratory at the Department of Reproductive Medicine, SU, in conjunction with infertility investigations and IVF/ICSI treatments. Usually, up to 2 mL of ejaculated sperm sample undergo gradient centrifugation, separating motile sperm from seminal plasma, immotile sperm, squamous epithelial cells, leukocytes, and bacteria. A portion of the pellet containing motile sperm is used to analyze sample parameters, primarily concentration and motility. During IVF/ICSI treatments, parts of the sperm sample are utilized for egg fertilization while the remainder is discarded. Following gradient centrifugation, sperm samples are diluted with a preservation liquid (ThinPrep®, 1:2) and stored in a refrigerator for transport to the Clinical Microbiology Department (virological laboratory) at SU (once per week) for polymerase chain reaction (PCR) analysis. ThinPrep® is routinely used to preserve and fix cell samples for HPV analysis in women. In this study, the portion of the sperm sample typically discarded and not used for IVF treatment will be utilized for HPV DNA analysis using PCR. PCR is the method routinely employed at the Clinical Microbiology Department (virological laboratory) at SU for HPV DNA detection in cervical cell samples. Results from these analyses will be correlated with sample parameters and the embryological outcome following completed IVF/ICSI treatment. Once analyzed by PCR and upon the availability of material, the samples will be stored for 5 years at Biobank Väst for potential future analyses of HPV-related biomarkers.
- Conditions
- Human Papilloma Virus, Infertility, Male
- Being tested
- HPV exposure
- Medical subject headings
- Infertility, Male
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HPV exposureOther
According to group descriptions
| Study group | Role | What they receive |
|---|---|---|
| Men with HPV-positive (HPV+) semen samples | Not described Receives: Other: HPV exposure | |
| Men with HPV-negative (HPV-) semen samples | Not described Receives: Other: HPV exposure |
What is being measured
The primary outcome is the main question the study is designed to answer.
Prevalence of HPV+ sperm samples
Number of HPV + sperm samples among all recruited men undergoing infertility treatment with IVF/ICSI
Measured: January 2023-March 2024
Secondary outcomes (5)
Semen volume in mL
Is semen volume different between men with HPV+ and HPV- semen samples?
Measured: January 2023-March 2024
Sperm concentration in number of spermatozoa/mL
Is sperm concentration different between men with HPV+ and HPV- semen samples?
Measured: January 2023-March 2024
Sperm motility in % of motile sperm
Is sperm motility different between men with HPV+ and HPV- semen samples?
Measured: January 2023-March 2024
Fertilization rate
Is the fertilization rate (number of fertilized oocytes) after IVF/ICSI treatment different between men with HPV+ and HPV- semen samples?
Measured: January 2023-March 2024
High quality embryos
Is the number of high-quality embryos(number of blastocysts developed after fertilization) after IVF/ICSI treatment different between men with HPV+ and HPV- semen samples?
Measured: January 2023-March 2024
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Dec 2023
- Study start1 Jan 2023
- Primary completion30 Jan 2024
- Study completion28 Mar 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Human Papilloma VirusStudies of the same condition, open and under way.
- More trials run by Vastra Gotaland RegionThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 260 participants (actual)
Sponsor and investigators
- Lead sponsor
- Vastra Gotaland Region
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Panagiotis Tsiartas, MD, PhD, Vastra Gotaland Region
- Investigators
- Randa Akouri, Ph.D., Principal investigator, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06161727
- Sponsor's protocol ID
- SpermHPV
- Status last verified
- Apr 2024
- First submitted
- 28 Nov 2023
- Last updated
- 26 Apr 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Francis J, Karrberg C, Hermansson J, Lindh M, Ganidou S, Thurin-Kjellberg A, Lundin K, Akouri R, Tsiartas P. Seminal HPV detection: a pilot study comparing the preservation effectiveness and cost between a methanol-based solution and cryopreservation with liquid nitrogen. Asian J Androl. 2022 Sep-Oct;24(5):560-561. doi: 10.4103/aja202213. No abstract available.
PubMed 35488669Francis J, Tsiartas P, Hreinsson J, Andersson M, Hermansson J, Gogas P, Papadimitriou T, Karrberg C, Brannstrom M, Akouri R. Semen HPV and IVF: insights from infection prevalence to embryologic outcomes. J Assist Reprod Genet. 2025 Jun;42(6):2053-2066. doi: 10.1007/s10815-025-03513-6. Epub 2025 May 22.
PubMed 40402400
Study at a glance
From the registry record, last updated by the sponsor on 26 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Detection and Prevalence of Human Papillomavirus (HPV) in Seminal Plasma and/or on Sperm in Men Undergoing Treatment With IVF/ICSI in Southwestern Sweden: a Prospective Study.
- ClinicalTrials.gov ID
- NCT06161727
- Acronym / sponsor ID
- SpermHPV
- Conditions
- Human Papilloma Virus, Infertility, Male
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 260 participants (actual)
- Lead sponsor
- Vastra Gotaland RegionOther government
- Study start
- 1 Jan 2023 (actual)
- Primary completion
- 30 Jan 2024 (actual)
- Study completion
- 28 Mar 2024 (actual)
- First posted
- 8 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This observational study aims to investigate the presence of HPV DNA in semen samples from men undergoing in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) treatment. It focuses on understanding the impact of HPV on male fertility and embryo development following IVF/ICSI. The primary goal is to determine the prevalence of HPV-positive (HPV+) semen samples among men seeking infertility treatment with IVF/ICSI. Additionally, the study aims to compare semen characteristics between HPV-positive and HPV-negative (HPV-) samples and assess the embryological outcomes after IVF/ICSI in these two groups.
Participants in this study will include men receiving IVF/ICSI treatment and providing fresh ejaculated sperm at Sahlgrenska University Hospital in Gothenburg, Sweden, over one year. Those undergoing treatments with surgically extracted sperm, sperm freezing for fertility preservation, or planning treatments involving preimplantation genetic testing or egg donation will be excluded.
The study will involve analyzing HPV DNA in semen samples through PCR, utilizing the most effective method for HPV DNA detection previously identified in a pilot study. Sperm samples collected during infertility investigations and IVF/ICSI treatments will undergo gradient centrifugation to separate different components. A portion of the sperm sample will be preserved for PCR analysis to detect HPV DNA, while the rest will be used for IVF/ICSI procedures. The results from the PCR analyses will be correlated with semen characteristics and the outcomes of IVF/ICSI treatment. Furthermore, the samples will be stored for potential future analyses related to HPV-related biomarkers for up to 5 years at Biobank.
Detailed description
Infection with the human papillomavirus (HPV) represents one of the most widespread sexually transmitted diseases, affecting both genders. Over 100 types of HPV can cause infections in the skin or mucous membranes and are typically transmitted through skin-to-skin contact, vaginal or anal intercourse, as well as oral sex. Statistics indicate that between 50 and 80 percent of sexually active adults will experience genital HPV infections during their lifetime. These infections tend to be persistent, especially in men. Although most HPV infections are asymptomatic, they can lead to genital warts, dysplasia, cancer, infertility, and may impact the outcomes of in vitro fertilization (IVF). Despite extensive research on HPV-related conditions in women, there has been limited attention given to HPV-related conditions in men.
A systematic review and meta-analysis conducted in 2017, comprising 31 studies, revealed that the prevalence of HPV DNA in semen samples among men in the general population was 11.4%, rising to 20.4% among men with infertility. It remains unclear whether HPV localizes in seminal plasma or in cellular fractions of semen samples (such as sperm, epithelial cells, or leukocytes). Recent evidence has shown that HPV DNA can be found on the surface of sperm by binding to specific glycosaminoglycans (GAGs), such as syndecan-1, along the equatorial region of the sperm head. Additionally, a few in vitro studies have indicated that HPV DNA can be found inside sperm when mixed with the HPV virus. The potential effects of HPV on fertility are not yet fully understood. The presence of HPV infection in sperm has been associated with impaired sperm parameters, mainly sperm motility, and increased sperm DNA fragmentation. Existing evidence suggests a negative effect of HPV DNA in seminal plasma and/or on sperm on the number of live births and ongoing pregnancies, although the level of evidence remains limited. Considering that sperm is utilized in IVF, it is crucial to investigate the presence of HPV in seminal plasma and sperm in these men, as well as any potential consequences on embryo development following IVF.
The primary objective of this study is to assess the prevalence of HPV DNA in seminal plasma and/or on sperm in men undergoing in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) treatments. Furthermore, the study aims to characterize semen parameters in men with HPV-positive (HPV+) and HPV-negative (HPV-) semen samples and analyze the embryological outcomes after IVF/ICSI in men with HPV+ semen samples compared to men with HPV- semen samples.
The secondary objectives include evaluating semen parameters such as volume, sperm concentration, and motility to determine if there are differences between men with HPV+ and HPV- semen samples. Additionally, the study aims to investigate whether the embryological outcome (fertilization rate, number of high-quality embryos) after IVF/ICSI treatment differs between men with HPV+ and HPV- semen samples.
Analyses of HPV DNA in seminal plasma and/or on sperm will be conducted using the method that has demonstrated the highest performance in detecting HPV DNA, based on a previously conducted pilot study. Sperm samples are typically provided at the Fertility Laboratory at the Department of Reproductive Medicine, SU, in conjunction with infertility investigations and IVF/ICSI treatments. Usually, up to 2 mL of ejaculated sperm sample undergo gradient centrifugation, separating motile sperm from seminal plasma, immotile sperm, squamous epithelial cells, leukocytes, and bacteria. A portion of the pellet containing motile sperm is used to analyze sample parameters, primarily concentration and motility. During IVF/ICSI treatments, parts of the sperm sample are utilized for egg fertilization while the remainder is discarded. Following gradient centrifugation, sperm samples are diluted with a preservation liquid (ThinPrep®, 1:2) and stored in a refrigerator for transport to the Clinical Microbiology Department (virological laboratory) at SU (once per week) for polymerase chain reaction (PCR) analysis. ThinPrep® is routinely used to preserve and fix cell samples for HPV analysis in women. In this study, the portion of the sperm sample typically discarded and not used for IVF treatment will be utilized for HPV DNA analysis using PCR. PCR is the method routinely employed at the Clinical Microbiology Department (virological laboratory) at SU for HPV DNA detection in cervical cell samples. Results from these analyses will be correlated with sample parameters and the embryological outcome following completed IVF/ICSI treatment. Once analyzed by PCR and upon the availability of material, the samples will be stored for 5 years at Biobank Väst for potential future analyses of HPV-related biomarkers.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Men with HPV-positive (HPV+) semen samples | – | Other: HPV exposure |
| Men with HPV-negative (HPV-) semen samples | – | Other: HPV exposure |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- Male only
- Age groups
- Adult
- Study population
- Men undergoing infertility treatment with IVF/ICSI and fresh ejaculated sperm at Sahlgrenska University Hospital (SU), Gothenburg, Sweden.
Key inclusion criteria (1 listed)
- Over the course of one year, the study will include men undergoing infertility treatment with IVF/ICSI and fresh ejaculated sperm at Sahlgrenska University Hospital (SU), Gothenburg, Sweden.
Key exclusion criteria (4 listed)
- Men undergoing IVF/ICSI treatments with surgically extracted sperm.
- Men undergoing sperm freezing for fertility preservation purposes or possessing previously frozen sperm.
- Sperm donors.
- Men for whom treatment with preimplantation genetic testing (PGT) or egg donation is planned.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| HPV exposureAccording to group descriptions | Other | Men with HPV-negative (HPV-) semen samples, Men with HPV-positive (HPV+) semen samples |
Primary outcome
Prevalence of HPV+ sperm samples
Time frame: January 2023-March 2024
Number of HPV + sperm samples among all recruited men undergoing infertility treatment with IVF/ICSI
5 secondary outcomes
Semen volume in mL
Time frame: January 2023-March 2024
Sperm concentration in number of spermatozoa/mL
Time frame: January 2023-March 2024
Sperm motility in % of motile sperm
Time frame: January 2023-March 2024
Fertilization rate
Time frame: January 2023-March 2024
High quality embryos
Time frame: January 2023-March 2024
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Apr 2024.
- Results publication: PubMed 35488669Francis J, Karrberg C, Hermansson J, Lindh M, Ganidou S, Thurin-Kjellberg A, Lundin K, Akouri R, Tsiartas P. Seminal HPV detection: a pilot study comparing the preservation effectiveness and cost between a methanol-based solution and cryopreservation with liquid nitrogen. Asian J Androl. 2022 Sep-Oct;24(5):560-561. doi: 10.4103/aja202213. No abstract available.
- Derived from this study: PubMed 40402400Francis J, Tsiartas P, Hreinsson J, Andersson M, Hermansson J, Gogas P, Papadimitriou T, Karrberg C, Brannstrom M, Akouri R. Semen HPV and IVF: insights from infection prevalence to embryologic outcomes. J Assist Reprod Genet. 2025 Jun;42(6):2053-2066. doi: 10.1007/s10815-025-03513-6. Epub 2025 May 22.
- Individual participant dataSharing planned: No
Related trials for Human Papilloma Virus
Not yet recruitingPhase 1/2
Clinical Trial to Assess the Safety, Tolerability, Reactogenicity, and Immunogenicity of a 10 Valent Human Papillomavirus Virus (10vHPV) Vaccine
Human Papillomavirus Infection
Active, not recruitingPhase 4
Comparing Immune Response of 2 vs 3 HPV Doses (27-45 Years Old)
Immunization, HPV Infection
Not yet recruitingPhase 2
Combination Bevacizumab and PRGN-2012 in Adults With Recurrent Respiratory Papillomatosis (RRP)
Respiratory Recurrent Papillomatosis (RRP), Human Papillomavirus (HPV)
RecruitingPhase 2
A Study of the Preliminary Efficacy of DARE-HPV to Treat High-risk Persistent Human Papillomavirus (hrHPV)
Human Papilloma Virus (HPV), High-risk Human Papillomavirus Infection
RecruitingPhase 2
A Single Arm Phase II Trial in p16-positive Oropharynx Cancer of Selective Dose De-escalation of nodAl VolumEs at Minimal Risk and Primary Site Disease (SAVED)
Head and Neck Cancer, Head and Neck Squamous Cell Cancer
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Randa Akouri, Ph.D. principal investigator
Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Human Papilloma Virus and Infertility, Male, run by Vastra Gotaland Region at 1 site in Sweden.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Prevalence of HPV+ sperm samples (time frame: January 2023-March 2024). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06161727, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Apr 2024.