<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chandwe K</submitter><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><pagination>2910</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11024201</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Malnutrition underlies almost half of all child deaths globally. Severe Acute Malnutrition (SAM) carries unacceptable mortality, particularly if accompanied by infection or medical complications, including enteropathy. We evaluated four interventions for malnutrition enteropathy in a multi-centre phase II multi-arm trial in Zambia and Zimbabwe and completed in 2021. The purpose of this trial was to identify therapies which could be taken forward into phase III trials. Children of either sex were eligible for inclusion if aged 6-59 months and hospitalised with SAM (using WHO definitions: WLZ &lt;-3, and/or MUAC &lt;11.5 cm, and/or bilateral pedal oedema), with written, informed consent from the primary caregiver. We randomised 125 children hospitalised with complicated SAM to 14 days treatment wi</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Malnutrition enteropathy in Zambian and Zimbabwean children with severe acute malnutrition: A multi-arm randomized phase II trial.</pubmed_title><pmcid>PMC11024201</pmcid><funding_grant_id>MR/P024033/1</funding_grant_id><funding_grant_id>220566/Z/20/Z</funding_grant_id><funding_grant_id>108065/Z/15/Z</funding_grant_id><pubmed_authors>Playford RJ</pubmed_authors><pubmed_authors>Hill S</pubmed_authors><pubmed_authors>Amadi B</pubmed_authors><pubmed_authors>Sonkwe H</pubmed_authors><pubmed_authors>Sauramba V</pubmed_authors><pubmed_authors>VanBuskirk K</pubmed_authors><pubmed_authors>Chipunza M</pubmed_authors><pubmed_authors>Tawodzera G</pubmed_authors><pubmed_authors>Ngosa D</pubmed_authors><pubmed_authors>Mutasa B</pubmed_authors><pubmed_authors>Dzikiti A</pubmed_authors><pubmed_authors>Murch SH</pubmed_authors><pubmed_authors>Chulu N</pubmed_authors><pubmed_authors>Mutasa K</pubmed_authors><pubmed_authors>Kelly P</pubmed_authors><pubmed_authors>Langhaug L</pubmed_authors><pubmed_authors>Prendergast AJ</pubmed_authors><pubmed_authors>Chandwe K</pubmed_authors><pubmed_authors>Sturgeon JP</pubmed_authors><pubmed_authors>Mudzingwa S</pubmed_authors><pubmed_authors>Makuyana R</pubmed_authors><pubmed_authors>Bwakura-Dangarembizi M</pubmed_authors><pubmed_authors>Kazhila L</pubmed_authors><pubmed_authors>Besa E</pubmed_authors><pubmed_authors>Zyambo K</pubmed_authors><pubmed_authors>Simunyola B</pubmed_authors><pubmed_authors>Zyambo M</pubmed_authors><pubmed_authors>Mudenda V</pubmed_authors><pubmed_authors>Mulenga C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Malnutrition enteropathy in Zambian and Zimbabwean children with severe acute malnutrition: A multi-arm randomized phase II trial.</name><description>Malnutrition underlies almost half of all child deaths globally. Severe Acute Malnutrition (SAM) carries unacceptable mortality, particularly if accompanied by infection or medical complications, including enteropathy. We evaluated four interventions for malnutrition enteropathy in a multi-centre phase II multi-arm trial in Zambia and Zimbabwe and completed in 2021. The purpose of this trial was to identify therapies which could be taken forward into phase III trials. Children of either sex were eligible for inclusion if aged 6-59 months and hospitalised with SAM (using WHO definitions: WLZ &lt;-3, and/or MUAC &lt;11.5 cm, and/or bilateral pedal oedema), with written, informed consent from the primary caregiver. We randomised 125 children hospitalised with complicated SAM to 14 days treatment wi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-01T10:48:38.737Z</modification><creation>2026-04-08T11:37:33.043Z</creation></dates><accession>S-EPMC11024201</accession><cross_references><pubmed>38632262</pubmed><doi>10.1038/s41467-024-45528-0</doi></cross_references></HashMap>