[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Southern Illinois University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":71},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100553932","phase-4-oral-iron-supplementation-on-alternate-vs-consecutive-days-for-iron-deficiency-anemia-in-pregnancy-100553932",false,"NCT06492512","Oral Iron Supplementation on Alternate vs. Consecutive Days for Iron Deficiency Anemia in Pregnancy","Inclusion Criteria:\n\n* Pregnant patients will be enrolled at less than 30 weeks gestational age (GA) with laboratory confirmed IDA (as defined by hemoglobin under 10.5 g\u002FdL, as well as ferritin under 15 mcg\u002FL)\n\nExclusion Criteria:\n\n* Patients \\\u003C18 years old, patients who have severe IDA that requires blood transfusion or IV iron infusion, patients who have other known hemoglobinopathy (such as thalassemia or sickle cell anemia) or anemia of different mechanism (such as vitamin B12 or folate deficiency), patients with ulcerative colitis, Crohn's disease, gastric ulcers, patients who have previously undergone gastric bypass surgery, patients who experience admission for antepartum bleed, have been diagnosed with abnormal placentation (i.e., placenta previa, placenta accreta, placenta increta or percreta)","FEMALE","18 Years","45 Years",{"count":19,"type":20},120,"ESTIMATED","INTERVENTIONAL",[23],"PHASE4","This will be a randomized clinical trial. Enrolled subjects will be randomized (1:1) into two study arms to receive either daily (Group 1) or alternate day (Group 2) supplementation with one oral pill containing ferrous sulfate with an equivalent elemental iron dose of 65 mg per pill.",[26,27],"Iron-deficiency Anemia (IDA)","Pregnancy",[29,30],"Iron-deficiency anemia (IDA)","Iron-deficiency anemia (IDA) during gestation","RECRUITING","2026-04-21",{"date":34,"type":35},"2026-04-24","ACTUAL",{"date":37,"type":35},"2025-05-27",{"date":39,"type":20},"2029-07-30",{"name":41,"class":42},"Southern Illinois University","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":57,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":65,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":43},"100522550","rural-illinois-lung-cancer-screening-initiative-100522550","NCT06084078","Rural Illinois Lung Cancer Screening Initiative","Patient Identification, Prescreening and LDCT Screening for Lung Cancer With Telehealth","LDCT","Inclusion Criteria:\n\n* All individuals 50-80 years of age\n* 20 pack-year smoking history\n* Currently smoke or have quit within the past 15 years:\n\nExclusion Criteria:\n\n* Individuals 49 years and below or 81 years and above\n* Has not smoked in 15 or more years\n* Individuals who develop a health problem that makes them unwilling or unable to have surgery if lung cancer is detected.","ALL","50 Years","80 Years",{"count":56,"type":20},10000,"30 Years","OBSERVATIONAL","The role of this observational study is to access the feasibility of providing lung cancer screening using a designated nurse navigator through lung cancer screening clinic. Eligible participants will be identified using medical records, eligibility will be confirmed through phone call, screening visits will be scheduled as in-person visit or telehealth visit. Computed tomography screening will be performed at an approved center closer to the individuals place of living and results will be discussed during follow-up in-person visit or telehealth visit.",[61],"Lung Cancer",[63,50,64],"cancer screening","Lung cancer",{"date":34,"type":35},{"date":67,"type":35},"2024-09-01",{"date":69,"type":20},"2030-08-31",{"name":41,"class":42},""]