[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100285792":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":18,"centralContacts":23,"locations":32,"responsibleParty":51,"collaborators":10,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":10,"eligibilityCriteria":58,"healthyVolunteers":59,"sex":60,"minAge":61,"maxAge":10,"enrollmentInfo":62,"targetDuration":10,"studyType":65,"phases":10,"briefSummary":66,"conditions":67,"keywords":70,"overallStatus":35,"whyStopped":10,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},{"fullName":5,"class":6},"National Institutes of Health Clinical Center (CC)","NIH",[8,12,15],{"label":9,"type":10,"description":11,"interventionNames":10},"1\u002FPatients",null,"Patients who underwent hematopoietic stem cell transplant for any indication (malignant or non-malignant).",{"label":13,"type":10,"description":14,"interventionNames":10},"2\u002FDonors","Related stem cell donors of those in Patients cohort.",{"label":16,"type":10,"description":17,"interventionNames":10},"3\u002FParents of patients","Parents\u002Fguardians of minors enrolled in cohort 1",[19],{"name":20,"affiliation":21,"role":22},"Najla El Jurdi, M.D.","National Cancer Institute (NCI)","PRINCIPAL_INVESTIGATOR",[24,29],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"Ashley E Carpenter","CONTACT","(240) 550-0492","carpentera@mail.nih.gov",{"name":20,"role":26,"phone":30,"phoneExt":10,"email":31},"(240) 992-4033","najla.eljurdi@nih.gov",[33],{"facility":34,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"National Institutes of Health Clinical Center","RECRUITING","Bethesda","Maryland","20892","United States","US",{"type":42,"coordinates":43},"Point",[44,45],-77.10026,38.98067,{"lat":45,"lon":44},[48],{"name":49,"role":26,"phone":50,"phoneExt":10,"email":10},"For more information at the NIH Clinical Center contact National Cancer Institute Referral Office","888-624-1937",{"type":52,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100285792","long-term-follow-up-of-patients-undergoing-hematopoietic-stem-cell-transplantation-cellular-therapy-or-gene-therapy-100285792",false,"NCT03000244","Long-Term Follow up of Patients Undergoing Hematopoietic Stem Cell Transplantation, Cellular Therapy, or Gene Therapy","* INCLUSION CRITERIA FOR PATIENT SUBJECTS:\n* Individuals who underwent HCT or received cellular or gene therapy for any indication (malignant or non-malignant) and are surviving one year or more from the date of therapy\n* Age \\>= 4 years\n* Ability of individual or individual s Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document\n* Individuals will need to have a primary physician within the US (primary care, oncologist, hematologist, etc.) that will provide continued comprehensive care for the duration of participation in the study. PI may allow for established medical providers to be located outside of the US.\n\nEXCLUSION CRITERIA FOR PATIENT SUBJECTS:\n\n-Individuals with active disease relapse or new hematologic malignancy including post-transplant lymphoproliferative disorder (PTLD) are excluded from protocol enrollment.\n\nINCLUSION CRITERIA FOR DONOR SUBJECTS:\n\n* Related stem cell donors of patients meeting the above criteria as a donor of hematopoietic progenitor and stem cells or leukocytes\n* Age \\>= 4years\n* Ability of patient or patient s Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document\n\nINCLUSION CRITERIA FOR PARENTS COMPLETING SURVEYS:\n\n* Parents\u002Fguardians of minors enrolled on the study who have undergone HCT\n* Willingness to complete surveys about the minor that underwent HCT",true,"ALL","4 Years",{"count":63,"type":64},2000,"ESTIMATED","OBSERVATIONAL","Background:\n\nPeople who have had an allogeneic hematopoietic stem cell transplant (HCT) have bone marrow or an immune system that is damaged. They get stem cells from a donor who is a relative. Researchers want to study stem cell donors and recipients to learn about the long-term effects of HCT. They want to learn how the stem cells change and how to improve their ability to fight cancer.\n\nObjective:\n\nTo provide long-term follow-up care for people who underwent or will undergo HCT. To collect data, blood, and tissue samples to learn about late complications after HCT.\n\nEligibility:\n\nAdults age 18 and older who will undergo HCT or underwent HCT and are surviving one year or more from the date of HCT. The stem cell donors for these recipients are also needed.\n\nDesign:\n\nRecipients will have 1 visit each year. They will have a physical exam. They will answer questions about their medical history and health. They will receive screening and surveillance testing. They will complete brief questionnaires.\n\nRecipients will have blood tests. They may have tissue biopsies or specimens (such as tissue in their cheek or skin or bone marrow biopsy).\n\nRecipients will give their current address and phone number, and the same data for one or two other people, who can get in contact with them.\n\nAfter the first visit at the clinic, some recipients may see a doctor close to home to get the necessary information and send it to NIH.\n\nDonors will come to the clinic for 1 visit. They will answer questions about their medical history. Blood samples will be taken.",[68,69],"Hematopoietic Stem Cell Transplantation","Tissue Donors",[71,72],"Natural History","HCT","2026-06-30",{"date":75,"type":76},"2026-07-01","ACTUAL",{"date":78,"type":76},"2017-04-26",{"date":80,"type":64},"2050-08-12",{"name":21,"class":6},1]