[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626268":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":29,"centralContacts":33,"locations":41,"responsibleParty":112,"collaborators":114,"id":118,"slug":119,"hasResults":120,"nctId":121,"briefTitle":122,"officialTitle":122,"acronym":123,"eligibilityCriteria":124,"healthyVolunteers":120,"sex":125,"minAge":126,"maxAge":127,"enrollmentInfo":128,"targetDuration":25,"studyType":131,"phases":132,"briefSummary":134,"conditions":135,"keywords":139,"overallStatus":63,"whyStopped":25,"lastUpdateSubmitDate":146,"lastUpdatePostDateStruct":147,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":155},{"fullName":5,"class":6},"Johns Hopkins Bloomberg School of Public Health","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Azithromycin","EXPERIMENTAL","Children 6-59 months with non-dysentery shigella diarrhea will be treated with Azithromycin 10 mg\u002Fkg once daily for 5 days.",[13],"Drug: Azithromycin",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo","PLACEBO_COMPARATOR","Children 6-59 months with non-dysentery Shigella diarrhea will receive placebo similar in appearance to the experimental drug once daily for 5 days.",[19],"Drug: Placebo",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","Azithromycin will be given as 10 mg\u002Fkg body weight once daily for 5 days",[9],null,{"type":22,"name":15,"description":27,"armGroupLabels":28,"otherNames":25},"Placebo will be similar in appearance to the intervention but will contain inactive ingredients.",[15],[30],{"name":31,"affiliation":5,"role":32},"Subhra Chakraborty, PhD, MPH, MSc","PRINCIPAL_INVESTIGATOR",[34,38],{"name":31,"role":35,"phone":36,"phoneExt":25,"email":37},"CONTACT","410-502-3154","schakr11@jhu.edu",{"name":39,"role":35,"phone":25,"phoneExt":25,"email":40},"Melissa Higdon, MPH","mhigdon@jhu.edu",[42,61,76,93],{"facility":43,"status":44,"city":45,"state":25,"zip":25,"country":46,"countryCode":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"icddr,b Matlab Hospital","NOT_YET_RECRUITING","Chāndpur","Bangladesh","BD",{"type":49,"coordinates":50},"Point",[51,52],90.65433,23.22714,{"lat":52,"lon":51},[55,59],{"name":56,"role":35,"phone":57,"phoneExt":25,"email":58},"Eva Sultana, MD","+8801641105930","eva.sultana1@icddrb.org",{"name":56,"role":60,"phone":25,"phoneExt":25,"email":25},"SUB_INVESTIGATOR",{"facility":62,"status":63,"city":64,"state":25,"zip":25,"country":46,"countryCode":47,"cosmosGeoPoint":65,"geoPoint":69,"contacts":70},"icddr,b Hospital","RECRUITING","Dhaka",{"type":49,"coordinates":66},[67,68],90.40744,23.7104,{"lat":68,"lon":67},[71,75],{"name":72,"role":35,"phone":73,"phoneExt":25,"email":74},"Sampa Dash, MD","+8801815858698","sampa.somc@gmail.com",{"name":72,"role":60,"phone":25,"phoneExt":25,"email":25},{"facility":77,"status":44,"city":78,"state":25,"zip":25,"country":79,"countryCode":80,"cosmosGeoPoint":81,"geoPoint":85,"contacts":86},"Matero Level 1 Hospital","Lusaka","Zambia","ZM",{"type":49,"coordinates":82},[83,84],28.28713,-15.40669,{"lat":84,"lon":83},[87,91],{"name":88,"role":35,"phone":89,"phoneExt":25,"email":90},"Chikumbutso Chipeta, M.D, MSc","+260969810681","chikumbutso.chipeta@cidrz.org",{"name":92,"role":60,"phone":25,"phoneExt":25,"email":25},"chikumbutso Chipeta, MD",{"facility":94,"status":44,"city":95,"state":25,"zip":25,"country":79,"countryCode":80,"cosmosGeoPoint":96,"geoPoint":100,"contacts":101},"Arthur Davidson Children's Hospital","Ndola",{"type":49,"coordinates":97},[98,99],28.63659,-12.95867,{"lat":99,"lon":98},[102,106,110],{"name":103,"role":35,"phone":104,"phoneExt":25,"email":105},"Sam Miti, BSc HB,MBcHB,MMed,FZCOM-PEDS","+260966292508","drsammiti@gmail.com",{"name":107,"role":35,"phone":108,"phoneExt":25,"email":109},"Mwizukanji Nachamba, MD","+260961950900","mwizukanjinachamba@gmail.com",{"name":111,"role":60,"phone":25,"phoneExt":25,"email":25},"Sam Miti, MD",{"type":113,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR",[115],{"name":116,"class":117},"National Institute of Allergy and Infectious Diseases (NIAID)","NIH","100626268","phase-2-the-impact-of-shigellosis-and-recommended-treatment-in-children-100626268",false,"NCT07433426","The Impact of Shigellosis and Recommended Treatment in Children","TrtNDSD","Inclusion Criteria:\n\n* Patients \\>6 and ≤59 months of age seeking care in the study hospitals\n* Patients residing within the study catchment area\n* Present with watery diarrhea and positive for Shigella by RLDT\n* Willing to be available for sample and data collection during the follow up visits\n\nExclusion Criteria:\n\n* Inability or unwillingness of a participant's parent\u002Fguardian to give written informed consent or comply with study protocol\n* Diarrhea started more than 96 hours before enrollment\n* Antibiotics related to shigellosis treatment (including the investigational drug azithromycin) taken in the past 5 days\n* More than 2 doses of antidiarrheal drugs taken in the past 24 hours\n* History of allergy to Azithromycin\n* Presence of visible blood in stool\n* Children with severe acute malnutrition (below -3z scores of the median WHO growth standards).\n* History of congenital heart diseases, known gastrointestinal abnormalities, including short bowel syndrome, chronic (inflammatory or irritable) bowel disease, inherited or acquired immune system deficiency rendering the patient immunocompromised, including chronic\u002Flong-term steroid treatment or other immunosuppressive treatment\n* Fever over 39°C (102°F) with other complications that require antibiotic treatment\n* Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study","ALL","6 Months","59 Months",{"count":129,"type":130},700,"ESTIMATED","INTERVENTIONAL",[133],"PHASE2","The purpose of this study is to evaluate whether antibiotic treatment of non-dysentery Shigella associated watery diarrhea (NDSD) cases improves clinical outcomes and growth in children.\n\nChildren with NDSD seeking care for diarrhea at the study hospitals in Bangladesh and Zambia will be enrolled and randomized to receive Azithromycin or placebo (a look-alike substance that contains no drug). Enrolled children will be followed for three months with household visits.\n\nThe investigators will determine whether antibiotic treatment of NDSD reduces the duration of diarrhea and time to microbiological cure (shedding of Shigella in stool), and whether it improves growth in children compared with the placebo group.",[136,137,138],"Diarrhea Infectious","Shigella","Growth & Development",[140,141,142,143,144,9,145],"shigella","children","randomized clinical trial","weight for age","growth outcomes","Diarrhea","2026-03-27",{"date":148,"type":149},"2026-03-30","ACTUAL",{"date":151,"type":149},"2026-03-18",{"date":153,"type":130},"2030-08",{"name":5,"class":6},4]