[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Perelel Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100616283","mom-multi-postnatal-supplementation-trial-100616283",false,"NCT07303595","Mom Multi Postnatal Supplementation Trial","Effect of a Postpartum Multivitamin-Mineral Supplement on Maternal Nutrient Status and Wellbeing","Inclusion criteria:\n\n* Healthy, postpartum women (\\~4 weeks \\[± 2 weeks\\]) with infants born term and singleton\n* Not pregnant during the study period\n* Able to understand (written and spoken) English or Spanish.\n\nExclusion criteria:\n\n* Cardiometabolic disease\n* Past pregnancy complications (gestational diabetes, hypertension)\n* malabsorption syndromes (IBS, IBD, Crohn's, Colitis, Celiac)\n* Caily use of medications which may affect nutrient absorption\n* chronic alcohol use (\\> 4 alcoholic drinks\u002Fday)\n* those prescribed postnatal MVM supplements by their physician\n* unwilling to discontinue dietary supplementation containing any of the active components in the study product over the study period\n* Women should not have an allergy or intolerance to active or inactive product ingredients.","FEMALE","18 Years",{"count":19,"type":20},80,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to learn if a vitamin and mineral supplement designed specifically for women after childbirth can improve their nutrition and health in women who are pregnant or have recently given birth (within 6 weeks).\n\nThe main question it aims to answer is:\n\nCan a postpartum-specific vitamin and mineral supplement help improve nutritional status and health outcomes in women after giving birth?\n\nResearchers will compare women who take the new postpartum vitamin and mineral supplement to women who take a placebo (fake pills without active ingredients) to see if the supplement improves their nutritional health.\n\nParticipants will:\n\nAttend 2 visits at University of Georgia (1-1.5 hours each) over 12 weeks Participate in 2 phone calls between visits Stop taking other vitamin\u002Fmineral supplements during the study Have blood drawn to test vitamin and mineral levels Provide urine samples and breastmilk samples if breastfeeding (optional) Have height, weight, and skin color measured Complete questionnaires about health, pregnancy, and mental wellness Answer questions about daily food and drink intake Take either the study supplement or placebo daily",[26],"Postnatal Care",[28,29],"Postnatal","multivitamin dietary supplement","RECRUITING","2025-12-10",{"date":33,"type":34},"2025-12-26","ACTUAL",{"date":36,"type":34},"2025-11-10",{"date":38,"type":20},"2026-10",{"name":40,"class":41},"Perelel Inc.","INDUSTRY",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":42},"100610348","prenatal-study-in-healthy-pregnant-women-100610348","NCT07226414","Prenatal Study in Healthy Pregnant Women","Evaluating the Impact of Perelel Prenatal on Biomarkers in Healthy Pregnant Women.","Inclusion Criteria:\n\n* Be able to give written informed consent.\n* Healthy pregnant women between 21- 40 years of age (inclusive).\n* Pregnant women in the second trimester of pregnancy (gestational age of 14-19 weeks).\n* Willing to consume the Study Product daily for the duration of the study.\n\nExclusion Criteria:\n\n* History of drug or alcohol abuse\n* Is hypersensitive to any of the contents of the study product, that would preclude intake of the study products.\n* Has any significant acute or chronic coexisting health conditions that would prevent them from fulfilling the study requirements, put the Participant at risk, or would confound the interpretation of the study results as judged by the investigator on the basis of medical history.\n* Severe nausea and vomiting in the first trimester, including hyperemesis gravidarum (HG)\n* Inability to tolerate oral supplement intake due to gastrointestinal symptoms during the first trimester of pregnancy\n* Prior Pregnancy Complications (gestational diabetes (GD), HG, or pre-eclampsia, NTDs (Neural Tube Defects))\n* Current pregnancy complications (GD, Iron Deficiency Anemia)\n* Hypertension\n* Diabetes mellitus\n* Cardiovascular disease\n* Class II\u002FIII obesity (defined as BMI ≥35.0 Kg\u002Fm2)\n* Malabsorption syndromes (e.g., celiac disease, inflammatory bowel disease)\n* Severe anemia or iron overload disorders\n* Thyroid disorders\n* Current or recent (in the past 12 weeks prior to Visit 1) use of a medication that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results, as judged by the investigator. Prohibited medications include:\n\nMedications that contain fat-soluble vitamins A, E, or K in high doses\n\n\\- Current or recent (in the past 12 weeks prior to Visit 1) use of prohibited nutritional or non-nutritional supplements that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results as judged by the investigator.","21 Years","40 Years",{"count":53,"type":20},40,[23],"Clinical Trial Summary\n\nThe goal of this clinical trial is to address the impact of a gummy prenatal vs a capsule based prenatal in pregnant women. The main question it aims to answer is:\n\nDoes 12-week daily administration of Prenatal Capsule affect serum iron levels in pregnant women in their second trimester compared to a comparator gummy prenatal?\n\nResearchers will compare Prenatal Capsule to a comparator Prenatal Gummy to see if there are differences in serum iron levels after 12 weeks of daily use.\n\nParticipants will:\n\nTake their assigned prenatal supplement (either Prenatal Capsule or the comparator Prenatal Gummy) daily for 12 weeks Be in their second trimester of pregnancy during the study period Have their serum iron levels measured at baseline and after the 12-week intervention period",[57],"Pregnancy",{"date":59,"type":34},"2025-12-18",{"date":61,"type":34},"2025-12-01",{"date":63,"type":20},"2026-11",{"name":40,"class":41},""]