[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100655351":3},{"organization":4,"outcomesModule":7,"designInfo":41,"detailedDescription":45,"studyPopulation":46,"armGroups":47,"interventions":42,"overallOfficials":42,"centralContacts":42,"locations":57,"responsibleParty":76,"collaborators":78,"id":81,"slug":82,"hasResults":83,"nctId":84,"briefTitle":85,"officialTitle":85,"acronym":42,"eligibilityCriteria":86,"healthyVolunteers":87,"sex":88,"minAge":89,"maxAge":90,"enrollmentInfo":91,"targetDuration":42,"studyType":94,"phases":42,"briefSummary":95,"conditions":96,"keywords":102,"overallStatus":59,"whyStopped":42,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":120},{"fullName":5,"class":6},"IVI Murcia","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":36},[9],{"measure":10,"description":11,"timeFrame":12},"Sperm DNA methylation profile","DNA methylation levels of a predefined nine-gene panel measured by pyrosequencing with duplicate measurements and compared between fresh, slow-frozen, and vitrified sperm samples.","Baseline (study semen collection visit) and after thawing of cryopreserved semen samples, through study completion (up to 9 months).",[14,17,20,23,26,29,32],{"measure":15,"description":16,"timeFrame":12},"Sperm concentration","Sperm concentration (million sperm\u002FmL) measured using computer-assisted sperm analysis (CASA).",{"measure":18,"description":19,"timeFrame":12},"Total sperm motility","Percentage of motile sperm measured using CASA.",{"measure":21,"description":22,"timeFrame":12},"Progressive sperm motility","Percentage of progressively motile sperm measured using computer-assisted sperm analysis (CASA).",{"measure":24,"description":25,"timeFrame":12},"Normal sperm morphology","Percentage of sperm with normal morphology assessed by microscopic evaluation of stained slides according to World Health Organization (WHO) criteria.",{"measure":27,"description":28,"timeFrame":12},"Sperm DNA fragmentation","DNA fragmentation measured in fresh, slow-frozen, and vitrified sperm samples.",{"measure":30,"description":31,"timeFrame":12},"Sperm telomere length","Sperm telomere length measured in fresh, slow-frozen, and vitrified sperm samples.",{"measure":33,"description":34,"timeFrame":35},"Seminal plasma extracellular vesicle composition","Characterization of seminal plasma extracellular vesicle composition in fresh semen samples.","Baseline (study semen collection visit).",[37],{"measure":38,"description":39,"timeFrame":40},"Blood leukocyte telomere length","Blood cell telomere length measured to investigate its relationship with participant age and sperm molecular characteristics.","Baseline (study blood collection visit).",{"allocation":42,"interventionModel":42,"interventionModelDescription":42,"primaryPurpose":42,"observationalModel":43,"timePerspective":44,"maskingInfo":42},null,"COHORT","PROSPECTIVE","The aging process is associated with declining fertility and increased risks of adverse reproductive and offspring health outcomes. Although the effects of maternal age have been extensively studied, the impact of paternal aging on sperm quality, reproductive outcomes, and molecular characteristics of sperm remains incompletely understood.\n\nThe primary objective of this study is to evaluate whether sperm cryopreservation may serve as an alternative to the use of sperm collected at older ages in assisted reproduction treatments. The primary endpoint is the difference in sperm DNA methylation patterns between fresh ejaculated samples and samples subjected to cryopreservation. Cryopreservation will be considered a potentially valid strategy if DNA methylation patterns remain substantially preserved following the cryopreservation process.\n\nAt least 45 male participants will be recruited and grouped according to age. Participants will provide one semen sample and a peripheral blood sample. Following routine semen analysis, each semen sample will be divided into three aliquots: fresh, slow-frozen, and vitrified. Cryopreserved aliquots will be stored in liquid nitrogen and subsequently thawed or warmed for analysis.\n\nStandard semen parameters, including volume, concentration, motility, sperm kinetics, and morphology, will be evaluated. Additional analyses will include sperm DNA methylation, DNA fragmentation, telomere length, and characterization of extracellular vesicles and their composition. Identical assessments will be performed on fresh and cryopreserved samples to compare the effects of slow freezing and vitrification.\n\nSecondary objectives include evaluating age-related differences in semen quality and molecular biomarkers, identifying markers associated with biological gamete age, characterizing age-related differences in seminal extracellular vesicles, and exploring associations between sperm molecular characteristics and lifestyle. Participants will also complete validated questionnaires regarding lifestyle and dietary habits.","Adult men aged 18-65 years attending IVI Murcia for semen analysis, fertility assessment, semen donation, or assisted reproduction treatment who meet the study eligibility criteria and provide informed consent. Participants will provide semen and blood samples for laboratory assessment of sperm quality and molecular characteristics before and after cryopreservation.",[48,51,54],{"label":49,"type":42,"description":50,"interventionNames":42},"Men aged 18-39 years","Male participants aged 18-39 years who provide semen and blood samples for laboratory assessment of sperm quality and molecular characteristics. Semen samples are divided into fresh, slow-frozen, and vitrified aliquots for comparative analysis.",{"label":52,"type":42,"description":53,"interventionNames":42},"Men aged 40-49 years","Male participants aged 40-49 years who provide semen and blood samples for laboratory assessment of sperm quality and molecular characteristics. Semen samples are divided into fresh, slow-frozen, and vitrified aliquots for comparative analysis.",{"label":55,"type":42,"description":56,"interventionNames":42},"Men aged ≥50 years","Male participants aged 50 years and older who provide semen and blood samples for laboratory assessment of sperm quality and molecular characteristics. Semen samples are divided into fresh, slow-frozen, and vitrified aliquots for comparative analysis.",[58],{"facility":5,"status":59,"city":60,"state":60,"zip":61,"country":62,"countryCode":63,"cosmosGeoPoint":64,"geoPoint":69,"contacts":70},"RECRUITING","Murcia","30007","Spain","ES",{"type":65,"coordinates":66},"Point",[67,68],-1.13004,37.98704,{"lat":68,"lon":67},[71],{"name":72,"role":73,"phone":74,"phoneExt":42,"email":75},"Juan Carlos Martínez","CONTACT","+34 651 79 10 00","JuanCarlos.Martinez@ivirma.com",{"type":77,"investigatorFullName":42,"investigatorTitle":42,"investigatorAffiliation":42,"oldNameTitle":42,"oldOrganization":42},"SPONSOR",[79],{"name":80,"class":6},"European Union","100655351","human-sperm-cryopreservation-as-an-alternative-to-the-decline-of-sperm-quality-with-aging-100655351",false,"NCT07814235","Human Sperm Cryopreservation as an Alternative to the Decline of Sperm Quality With Aging","Inclusion Criteria:\n\n* Male participants aged 18 to 65 years\n* Attending IVI Murcia for semen analysis and\u002For assisted reproduction treatment\n* Able and willing to provide written informed consent\n* Willing to provide a semen sample and a blood sample for research purposes\n\nExclusion Criteria:\n\n* Previous diagnosis of azoospermia or severe oligozoospermia (sperm concentration \\\u003C1 million sperm\u002FmL)\n* Known chromosomal abnormality (abnormal karyotype)\n* Known Y chromosome microdeletion\n* Febrile illness within the previous 3 months\n* Presence of varicocele\n* Current use of vitamin or antioxidant supplements intended to improve semen quality",true,"MALE","18 Years","65 Years",{"count":92,"type":93},45,"ESTIMATED","OBSERVATIONAL","This observational study will evaluate whether sperm cryopreservation can help preserve sperm quality and molecular characteristics that may be affected by increasing paternal age. Men aged 18 years and older will provide a semen sample and a blood sample for laboratory analysis. Each semen sample will be divided into fresh, slow-frozen, and vitrified aliquots. The study will compare sperm quality (as assessed by computer-assisted sperm analysis), DNA methylation profiles, DNA fragmentation, sperm telomere length before and after cryopreservation. The effects of age on these parameters will also be assessed. The impact of age on seminal plasma extracellular vesicle composition and blood cell telomere length will also be analysed. The goal is to determine whether sperm cryopreservation may represent a strategy for preserving sperm characteristics associated with younger paternal age.",[97,98,99,100,101],"Aging","Epigenetic Aging","Infertility","Assisted Reproduction Technologies","Male Fertility",[103,104,105,106,107,108,109,110],"infertility","cryopreservation","sperm","semen","semen analysis","DNA methylation","epigenetics","assisted reproductive technology","2026-09-08",{"date":113,"type":114},"2026-09-10","ACTUAL",{"date":116,"type":114},"2026-06-10",{"date":118,"type":93},"2027-09-30",{"name":5,"class":6},1]