[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"nutrient-deficiency\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:nutrient-deficiency":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,41,73,105,136],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100580318","implementation-of-multiple-micronutrient-supplementation-mms-for-pregnant-women-in-uganda-100580318",false,"NCT06835738","Implementation of Multiple Micronutrient Supplementation (MMS) for Pregnant Women in Uganda","Inclusion Criteria for Pregnant women- Enrolled for follow-up throughout pregnancy (sample 1)\n\n* ≤24 weeks of amenorrhea\u002Fgestation as verified by health professionals\n* Attending first ANC visit at government or PNFP health facilities.\n* Accepted to take MMS at first ANC visit\n\nExclusion Criteria for Pregnant women- Enrolled for follow-up throughout pregnancy (sample 1)\n\n* Pregnant women with pre-existing hematological conditions such as sickle cell anemia, thalassemia, hemochromatosis.\n* Pregnant women planning to relocate outside the study district during the study period.\n\nInclusion Criteria for Pregnant women \u002F Women that have recently delivered (single contact) (sample 2)\n\n* Currently pregnant woman or a woman who is not more than 8 weeks postpartum.\n* Received MMS at an ANC visit at least 3 months ago or more.\n* Attended at least any 2 monthly ANC visits.\n* Attending\u002Fattended ANC at government or private-not-for-profit health facility.\n\nExclusion Criteria for Pregnant women \u002F Women that have recently delivered (single contact) (sample 2)\n\n* Enrolled in study population 1.\n* Women who are more than 8 weeks postpartum.\n\nInclusion Criteria for ANC providers having ANC health education\u002Fcounseling with pregnant woman(en) observed (sample 3)\n\n• Healthcare providers that are currently providing ANC health education (group) or ANC individual counseling at government or PNFP health facilities.\n\nExclusion Criteria for ANC providers having ANC health education\u002Fcounseling with pregnant woman(en) observed (sample 3) • Healthcare providers that are currently providing ANC health education (group) or ANC individual counseling to a woman(en) that have not provided written informed consent to have the ANC session observed.\n\nInclusion Criteria for Influential family members (male partners \\& mothers\u002Fmothers-in law) (sample 4)\n\n* Spouse or partner of a pregnant woman or woman with a child less than 8 weeks old who is receiving\u002F has received ANC services in one of the 8 study districts.\n* Mother or mother-in-law of a pregnant woman or woman with a child less than 8 weeks old who is receiving\u002F has received ANC services in one of the 8 study districts.\n\nExclusion Criteria for Influential family members (male partners \\& mothers\u002Fmothers-in law) (sample 4) • None\n\nInclusion Criteria for Healthcare Providers- including facility in-charge, ANC providers, Health Assistants, staff in-charge of records, and stores manager (sample 5)\n\n* Health workers who provide ANC services (e.g., midwives\u002Fnurse, medical\u002F clinical officers, health assistants, and nutrition focal person) at government or private-not-for-profit facilities in one of the 8 study districts.\n* Health facility staff (e.g., Facility In-charge, Maternity In-charge, Pharmacy\u002FStores In-charge) at government or private-not-for-profit facilities in one of the 8 study districts.\n\nExclusion Criteria for Healthcare Providers- including facility in-charge, ANC providers, Health Assistants, staff in-charge of records, and stores manager (sample 5)\n\n• None\n\nInclusion Criteria for Community Health Workers (VHTs) and Mentor Mothers (sample 6) • Voluntary Health Team (VHT), Mentor Mothers, or Para-socials attached to at least one of the study facilities.\n\nExclusion Criteria for Community Health Workers (VHTs) and Mentor Mothers (sample 6) • None\n\nInclusion Criteria for National, regional, and district-level stakeholders (sample 7)\n\n* National, regional, or district-level decision-makers working in nutrition, maternal, newborn and child health, district health educator or pharmaceutical roles associated with the antenatal care system in Uganda.\n* Implementing partners involved in direct implementation of MMS within the 8 study districts\n\nExclusion Criteria for National, regional, and district-level stakeholders (sample 7)\n\n• None\n\nInclusion Criteria for Pregnant women - interviewed during post-intervention Household Coverage Survey (sample 8)\n\n* Woman who has been pregnant or delivered within the study period.\n* Household is within one of the 4 selected districts.\n\nExclusion Criteria for Pregnant women - interviewed during post-intervention Household Coverage Survey (sample 8)\n\n• Women who moved to the district after delivery.",true,"ALL","0 Years","80 Years",{"count":20,"type":21},4077,"ESTIMATED","INTERVENTIONAL",[24],"NA","The objective of this research is to understand how antenatal multiple micronutrient supplements (MMS) can be effectively implemented and scaled within the Uganda national health system context to support improved maternal nutrition and birth outcomes. Formative research has been conducted to design the implementation strategies that will be tested in this second phase of the study. The objectives are to:\n\n* Describe the implementation of the MMS intervention (which consists of MMS product, a social behavior change communication (SBCC) strategy, capacity building, MMS supply chain support, monitoring, and evaluation) and explore acceptability, feasibility, fidelity, coverage, and potential for sustainability.\n* Determine the effect of dispensing MMS in different bottle counts on MMS adherence and ANC attendance among pregnant women.\n* Determine the cost and budget impact of MMS intervention implementation integrated in the Ugandan ANC service delivery system",[27],"Nutrient Deficiency","RECRUITING","2026-06-29",{"date":31,"type":32},"2026-07-01","ACTUAL",{"date":34,"type":32},"2025-06-18",{"date":36,"type":21},"2026-12-31",{"name":38,"class":39},"Johns Hopkins Bloomberg School of Public Health","OTHER",1,{"id":42,"slug":4,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":47,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":52,"briefSummary":54,"conditions":55,"keywords":61,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":40},"100613801","NCT07271316","Alii Supplement Study","Birth Control Supplement Study","Inclusion Criteria:\n\n* Participants must be on the hormonal birth control pill as the investigators are testing the effectiveness of a supplement for women who take the hormonal birth control pill\n* Participants must be willing to complete a follow up survey as this study will be multiple parts\n* Participants must be willing to take a daily supplement as this study is testing how a supplement influences a variety of psychological outcomes\n* Participants must be on the hormonal birth control pill for at least six months as participants who have been on the pill for less than 6 months may not be experiencing nutritional depletion yet\n* If the investigators are able to do so, the investigators will only recruit participants who take the one-month hormonal birth control pill rather than the three month hormonal birth control pill, as the investigators are going to have participants come in after 28 days (day 2 of pack 1 and day 2 of pack 2) and participants on the three-month HBC pill may be on a 21 day cycle.\n* Participants must have no food or medication allergies that will prevent the participants from safely taking the supplement\n* Participants must not be taking any vitamins or participant must report willingness to abstain from taking vitamins during the study as individuals who are already taking vitamins may not be experiencing nutritional depletion associated with hormonal birth control\n* If the investigators have the ability to do so, the investigators will only recruit participants who are not taking medications. Participants on various medications (e.g., SSRIs, ADHD medications, etc.) may report differing psychological states due to their medications, rather than the supplement. Therefore, it would be best to exclude those individuals if possible.\n\nExclusion Criteria:\n\n* Participants cannot be naturally cycling as the investigators are testing a supplement for women on hormonal birth control\n* Participants cannot be unwilling to complete a follow up study because this is a multi-part study\n* Participants cannot be unwilling to take a supplement because the study centers around taking a supplement\n* Participants cannot be on the hormonal birth control pill for less than 6 months as participants who have been on the pill for less than 6 months may not be experiencing nutritional depletion yet\n* If the investigators are able to do so, participants cannot take the three month hormonal birth control pill, as the investigators are going to have participants come in after 28 days (day 2 of pack 1 and day 2 of pack 2) and participants on the three-month HBC pill may be on a 21 day cycle.\n* Participants cannot have any food or medication allergies that will prevent the participants from safely taking the supplement\n* Participants must not be taking any vitamins or participants must report willingness to abstain from taking vitamins during the study as individuals who are already taking vitamins may not be experiencing nutritional depletion associated with hormonal birth control\n* If the investigators have the ability to do so, the investigators will only recruit participants who are not taking medications. Participants on various medications (e.g., SSRIs, ADHD medications, etc.) may report differing psychological states due to their medications, rather than the supplement. Therefore, it would be best to exclude those individuals if possible.","FEMALE","18 Years","25 Years",{"count":51,"type":21},68,[53],"PHASE2","The goal of this clinical trial is to learn if the Alii Supplement can be used to reduce symptoms related to nutritional depletion in hormonal birth control pill users. The main questions it aims to answer are:\n\nDoes usage of the supplement increase happiness, decrease perceived vulnerability to disease, increase digestive health, decrease mood swings, and increase energy?\n\nThe investigators will compare the Alii Supplement to a placebo (a capsule that contains no drug) to see if the Alii Supplement works to reduce symptoms associated with nutritional depletion.\n\nParticipants will:\n\nTake the placebo or Alii Supplement everyday for 28 days and visit the research office twice to fill out an online survey comprising of items examining the main outcome measures.",[27,56,57,58,59,60],"Happiness","Digestive Health","Vulnerability to Disease","Mood Swings","Energy",[62,63,64],"Hormonal Birth Control","Nutritional Depletion","Dietary Supplement","2026-01-12",{"date":67,"type":32},"2026-01-14",{"date":65,"type":32},{"date":70,"type":21},"2026-04-29",{"name":72,"class":39},"Texas Christian University",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":15,"sex":16,"minAge":48,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":85,"conditions":86,"keywords":90,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":40},"100486030","conversion-to-sadi-s-rygb-or-oagb-after-failed-sleeve-100486030","NCT05608772","Conversion to SADI-S, RYGB or OAGB After Failed Sleeve","Conversion of Failed Sleeve Gastrectomy Due to Weight Regain to SADI-S, RYGB or OAGB","RCTresleeve","Inclusion Criteria:\n\n* Undergone primary laparoscopic sleeve gastrectomy in the past\n* Weight regain\n\n  * defined as any increase in weight above the nadir as reported by the patient\n  * BMI at the time of revisional surgery was around 45 kg\u002Fm2\n  * weight regain was defined as an increase in BMI after bariatric surgery to exceed 35\n* With or without Gastroesophageal reflux disease (GERD) grade A and B o Patients with grade C or higher GERD, according to the Los Angeles (LA) classification \\[7\\] will be excluded from the study\n\nExclusion Criteria:\n\n* Didn't follow preoperative consultation\n* Cannot give of sign informed consent","60 Years",{"count":83,"type":21},234,[24],"Assess what revisional surgery is superior and provides the best weight loss after primary LSG. What is the occurrence of complications and the nutritional laboratory status? And if the resolution and \u002For improvement of associated medical problems after the weight loss will occur.",[87,88,89,27],"Weight Loss","Bariatric Surgery Candidate","Comorbidities and Coexisting Conditions",[91,92,93,94],"RYGB","OAGB","SADI-S","Sleeve gastrectomy","2025-09-10",{"date":97,"type":32},"2025-09-16",{"date":99,"type":32},"2023-03-15",{"date":101,"type":21},"2028-04-15",{"name":103,"class":104},"General Committee of Teaching Hospitals and Institutes, Egypt","OTHER_GOV",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":47,"minAge":48,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":114,"phases":4,"briefSummary":115,"conditions":116,"keywords":120,"overallStatus":126,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":4},"100519680","diet-quality-of-pregnant-women-with-a-strict-plant-based-diet-versus-an-omnivorous-diet-100519680","NCT06046703","Diet Quality of Pregnant Women With a Strict Plant-based Diet Versus an Omnivorous Diet","Diet Quality of Pregnant Women With a Strict Plant-based Diet Versus an Omnivorous Diet: a Focus on Vitamin B12 Intake and Other Nutritional and Pregnancy-related Outcomes","Inclusion Criteria:\n\n* Before 27 weeks of pregnancy\n* Age \\>18 years\n* Strict plant-based diet (vegan diet), defined as a diet without ingestion of animal products (i.e., intake less than once a month during) the entire pregnancy or omnivorous diet, defined as a diet that includes meat\n* Willing and able to give written informed consent and to understand, participate and comply with the research project requirements\n\nExclusion Criteria:\n\n* Food allergy that influences the nutritional intake, e.g., milk allergy, celiac disease, and lactose intolerance\n* Medical history of gastrointestinal diseases such as Crohn's disease and other diseases associated with vitamin B12 deficiencies such as (pre-existing) diabetes.\n* Medical history of abdominal surgery interfering with nutrient uptake, such as gastric bypass and intestinal resections\n* Pre-existing cardio-vascular diseases or auto-immune diseases\n* Insufficient understanding of the Dutch language",{"count":113,"type":21},256,"OBSERVATIONAL","The goal of this observational study is to compare the nutritional intake among pregnant women with a strict plant-based diet versus an omnivorous diet.\n\nThe main aim is to compare vitamin B12 intake.\n\nParticipants will be asked to:\n\n* fill out a health questionnaire\n* fill out a three-day food diary\n* undergo blood sampling Researchers will compare pregnant women with a strict plant-based diet and pregnant women with an omnivorous diet to see if their nutritional intake is comparable.",[117,118,27,119],"Vitamin B 12 Deficiency","Pregnancy","Dietary Exposure",[121,122,123,124,125],"vegan diet","pregnancy","vitamin b12","omnivorous","nutrition","NOT_YET_RECRUITING","2024-03-12",{"date":129,"type":32},"2024-03-13",{"date":131,"type":21},"2025-01-01",{"date":133,"type":21},"2027-07-01",{"name":135,"class":39},"Maastricht University Medical Center",{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":15,"sex":16,"minAge":143,"maxAge":144,"enrollmentInfo":145,"targetDuration":4,"studyType":22,"phases":147,"briefSummary":148,"conditions":149,"keywords":153,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":158,"lastUpdatePostDateStruct":159,"startDateStruct":161,"completionDateStruct":163,"leadSponsor":165,"locationsCount":40},"100518072","impact-evaluation-of-benazir-nashonuma-program-bnp-on-stunting-among-under-five-children-100518072","NCT06025786","Impact Evaluation of Benazir Nashonuma Program (BNP) on Stunting Among Under-five Children","Impact Assessment of Benazir Nashonuma Program (BNP) on Stunting Prevention Among Children 0-59 Months of Age in Pakistan","All those households are eligible to be included in the study who have:\n\n* An under-five child with a mother registered with Benazir Income Support Program (BISP)\n* Both available at the time of interview\n\nExclusion criteria includes:\n\n• Mother of the child who is not a woman of reproductive age, i.e., less than 15 years or greater than 49 years","1 Day","59 Months",{"count":146,"type":21},13200,[24],"The aim of the study is to evaluate the impact of Benazir Nashonuma Program (BNP) on prevalence of stunting among under-five children in low income setting of Pakistan. The research question that the study aims to answer is:\n\nIs there any change in the prevalence of stunting among under-five children in districts where Benazir Nashonuma Program (BNP) is established compared to districts where BNP is not established?\n\nDistricts where BNP is functional, and women and children are receiving the intervention will be compared at baseline and end line with control districts where conventional reproductive care services are given. Prevalence of stunting among under-five children will be compared along with other nutritional and growth status indicators over a period of 4 years.",[150,151,152,27],"Stunting","Wasting","Anemia",[154,155,150,151,156,157],"Quasi experimental study","Maternal and child nutrition","Under-five malnutrition","Specialized Nutritious Food (SNF)","2023-09-08",{"date":160,"type":32},"2023-09-11",{"date":162,"type":32},"2021-12-01",{"date":164,"type":21},"2026-06-30",{"name":166,"class":39},"Aga Khan University"]