[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100639095":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":20,"locations":10,"responsibleParty":26,"collaborators":10,"id":28,"slug":29,"hasResults":30,"nctId":31,"briefTitle":32,"officialTitle":33,"acronym":10,"eligibilityCriteria":34,"healthyVolunteers":30,"sex":35,"minAge":36,"maxAge":37,"enrollmentInfo":38,"targetDuration":10,"studyType":41,"phases":10,"briefSummary":42,"conditions":43,"keywords":48,"overallStatus":55,"whyStopped":10,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":10},{"fullName":5,"class":6},"AnnieGuard Corp.","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"PCOS Cohort",null,"Women aged 18 to 45 diagnosed with Polycystic Ovary Syndrome (PCOS) by a licensed healthcare provider. Participants complete an online questionnaire covering diagnosis history, symptoms, comorbidities, family history, current treatment, and self-reported lab values. Participants also submit copies of their lab results for verification. No intervention is administered.",[13],"Other: No intervention - observational data collection only",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"OTHER","No intervention - observational data collection only","This is an observational study. No intervention or treatment is administered. Participants submit existing lab results and clinical history through an online questionnaire.",[9],[21],{"name":22,"role":23,"phone":24,"phoneExt":10,"email":25},"Tiara Principal Investigator","CONTACT","240-234-0449","info@annieguard.com",{"type":27,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100639095","observational-study-on-the-causal-architecture-of-polycystic-ovary-syndrome-pcos-100639095",false,"NCT07623551","Observational Study on the Causal Architecture of Polycystic Ovary Syndrome (PCOS)","An Observational Data Collection Study to Characterize the Hormonal, Metabolic, and Clinical Architecture of Polycystic Ovary Syndrome in Women Aged 18 to 45: A Global Recruitment Initiative","Inclusion Criteria:\n\n* Female\n* Aged 18 to 45 years\n* Diagnosed with Polycystic Ovary Syndrome (PCOS) by a licensed healthcare provider\n* Willing to voluntarily share existing lab results and clinical history\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Under 18 years of age\n* Over 45 years of age\n* No confirmed PCOS diagnosis from a licensed healthcare provider\n* Unable or unwilling to provide informed consent","FEMALE","18 Years","45 Years",{"count":39,"type":40},100,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to learn about the causal architecture of Polycystic Ovary Syndrome (PCOS) in women aged 18 to 45. The main questions it aims to answer are:\n\nWhat does the hormonal, metabolic, and clinical architecture of PCOS look like across a diverse global population? Can the causal architecture of PCOS be reconstructed from existing lab results and clinical data? Are there distinct architectural patterns across different groups of women with PCOS? Participants who have been diagnosed with PCOS by a healthcare provider will complete an online questionnaire about their diagnosis, symptoms, clinical history, current treatment, and existing lab results. Participants will also be asked to submit copies of their most recent blood work and lab results. No intervention or treatment is involved. All data is de-identified.",[44,45,46,47],"Polycystic Ovary Syndrome","Polycystic Ovary Syndrome (PCOS)","PCOS","PCOS (Polycystic Ovary Syndrome)",[46,44,49,50,51,52,53,54],"Women's Health","Endocrine","Hormonal","Metabolic","Observational Study","Causal Architecture","NOT_YET_RECRUITING","2026-05-28",{"date":58,"type":59},"2026-06-03","ACTUAL",{"date":61,"type":40},"2026-06",{"date":63,"type":40},"2026-07",{"name":5,"class":6}]