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Rutf aprimorado pela membrana de gordura do leite para crianças com desnutrição aguda grave (MEND-SAM)

1 de novembro de 2026 atualizado por: Washington University School of Medicine

Rutf aprimorado por MFGM para crianças com Sam

The goal of this clinical trial is to test the use of milk fat globule membrane (MFGM) in ready-to-use therapeutic food (RUTF) in children with severe acute malnutrition in Sierra Leone. The main questions it aims to answer are:

  • Will the inclusion of MFGM in RUTF for 6-59-month-old Sierra Leonean children with severe acute malnutrition improve their neurodevelopment?
  • Will the inclusion of MFGM in RUTF for 6-59-month-old Sierra Leonean children with severe acute malnutrition reduce its worst consequences: death, hospitalization, and remaining severely malnourished despite treatment?

Researchers will compare the MFGM-containing RUTF to standard RUTF, which contains skim milk powder.

Participants will:

  • undergo measurement of length, weight, mid-upper arm circumference, and nutritional edema assessment every two weeks during severe malnutrition treatment
  • be treated with either MFGM-RUTF or standard RUTF at a dose of 2 sachets per day for up to 12 weeks
  • undergo neurodevelopmental testing using the Malawi Developmental Assessment Tool at the end of SAM treatment and 6 months later
  • a subset of participants will undergo blood spot collection and stool sample collection

Visão geral do estudo

Descrição detalhada

Globally, approximately 15 million children are suffering from severe acute malnutrition (SAM) at any one time, a number that has not declined in recent decades despite significant technological advancements in agriculture and food science. SAM is a condition of total-body depletion of the nutrients required for health and development; without treatment, 50% of affected children will die. Whereas historically children with SAM were admitted to and treated within hospitals, the advent of ready-to-use therapeutic food (RUTF) and community-based management of acute malnutrition revolutionized SAM care by allowing it to occur safely and successfully by the child's caregiver in their own home.

RUTF was designed to provide the nutrients required for physical recovery in a safe, palatable format. It is equal parts peanut paste, sugar, vegetable oil, and skim milk powder, with added micronutrients and emulsifier. At inception, attention was not specifically paid to how RUTF's composition might impact neurodevelopmental recovery in children with SAM. Research over the past decade has revealed that even following successful treatment with RUTF, children diagnosed with SAM still score 1-3 standard deviations below age-based expectations on neurodevelopmental tests. This suggests that the nutrient profile of standard RUTF is not sufficient to recover the developmental damage incurred by SAM.

Recently, progress has been made toward improving the developmental trajectory of children with SAM by altering RUTF. A randomized, blinded trial in Malawi including 2,500 children with SAM showed that improving the polyunsaturated fatty acid (PUFA) profile of RUTF by reducing linoleic acid and adding docosahexaenoic acid (DHA) yields superior neurodevelopment 6 months after treatment, by 0.19 standard deviations on a standardized, culturally adapted neurodevelopmental test. This demonstrates that neurodevelopmental recovery in SAM is sensitive to the lipid profile of RUTF. Despite the benefits of improved PUFA RUTF, however, children with SAM remained 1 standard deviation below expectations in neurodevelopment.

The milk fat globule membrane (MFGM) in mammalian milk contains a host of nutrients and bioactive compounds supportive of physical health and brain development. Bovine MFGM added to infant formula has been tested in several clinical trials and has demonstrated a reduction in infectious episodes, such as diarrhea and ear infections, as well as improvement in cognitive development, compared with infant formula not containing MFGM. In these trials and others, MFGM has been shown to be safe and well-tolerated. Currently, RUTF contains skim milk powder as its high-quality protein source, and peanut and vegetable oils as the primary sources of fat. These vegetable fat sources are deficient in the lipids provided by MFGM: sphingolipids, cholesterol, and other phospholipids such as phosphatidylcholine and phosphatidylethanolamine, all of which play roles in brain development. It is possible that the lipids contained in MFGM may further support neurodevelopmental recovery in SAM children.

By acting as a natural emulsifier, MFGM also offers a food formulation advantage that is relevant to children with SAM. Animal model studies have demonstrated that emulsifiers can compromise the gut barrier. Children with SAM have damaged small intestinal barrier function, which can lead to translocation of gut bacteria and resulting systemic infection. As RUTF will compose nearly 100% of a child's intake for the duration of treatment - up to 3 months - it is possible that inclusion of emulsifier may impede gut healing and recovery. Considering this concern, the Manary lab ran a clinical trial in 2018-2019 testing a novel formulation of RUTF designed with oat in place of some skim milk powder and peanut, and without hydrogenated vegetable oil (standard emulsifier), because oat acts as a natural emulsifier. In this trial, children with SAM receiving the oat-RUTF had 10% absolute higher recovery and a 33% relative reduction in the worst SAM outcomes (death, hospitalization, or remaining severely malnourished). Like oat, MFGM in RUTF allows for omission of emulsifier and may yield similar benefits.

Given (1) the repeated finding that adding MFGM to infant formulas improves neurodevelopment, (2) the impaired neurodevelopment of children with SAM, (3) the current RUTF formulation lacking neuro-supportive fats provided by MFGM, (4) MFGM's natural activity as an emulsifier, and (5), the reality that RUTF provides the sole source of nutrition for children with SAM, it is plausible that adding this high-quality source of lipids and protein to RUTF may also benefit children with SAM in both immediate and long-term physical and cognitive recovery.

This will be an individually randomized, investigator/outcomes assessors-blinded, controlled clinical trial designed to determine if treatment of severely malnourished Sierra Leonean children 6-59-months of age with an RUTF made with MFGM-containing whey protein/fat concentrate will (1) improve neurodevelopment and (2) reduce a composite of poor SAM outcomes (death, hospitalization, remaining severely malnourished), compared with standard RUTF (S-RUTF). This trial will be conducted at 20 rural sites in Sierra Leone. 1600 children will be randomized 1:1 to receive 2 sachets per day of either MFGM-RUTF or S-RUTF. Children will receive their allocated RUTF and return to clinic fortnightly for repeat anthropometric measurements, illness questions, and to receive more RUTF until they achieve a clinical outcome or for a maximum of 12 weeks, at which point they will undergo Malawi Developmental Assessment Tool (MDAT) testing. Participants will be asked to return to clinic 6 (5-7) months later for MDAT testing, the global z-score from which will be the trial's co-primary outcome. A subset of participants will undergo blood spot and/or stool sample collection at the end of SAM treatment.

Tipo de estudo

Intervencional

Inscrição (Estimado)

1600

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Pujehun
      • Bandajuma, Pujehun, Serra Leoa
        • Bandajuma
      • Bandasuma, Pujehun, Serra Leoa
        • Bandasuma
      • Bendu Malen, Pujehun, Serra Leoa
        • Bendu Malen
      • Gbondapi, Pujehun, Serra Leoa
        • Gbondapi
      • Jendema, Pujehun, Serra Leoa
        • Jendema
      • Potoru, Pujehun, Serra Leoa
        • Potoru
      • Pujehun, Pujehun, Serra Leoa
        • Static
      • Sahn Malen, Pujehun, Serra Leoa
        • Sahn Malen
      • Taninahun, Pujehun, Serra Leoa
        • Taninahun
      • Zimmi, Pujehun, Serra Leoa
        • Zimmi

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

6 meses a 4 anos (Filho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • 6-59 months of age
  • Reside within the catchment area of a participating clinic
  • mid-upper arm circumference < 11.5 cm and/or weight-for-length z-score < -3 and/or presence of bilateral pedal pitting edema
  • willingness to comply with all study procedures and availability for the duration of the study, including no plan to move from the catchment area of a participating clinic

Exclusion Criteria:

  • Features of complicated SAM: inability to tolerate a 30 g test dose of RUTF, breathing difficulties, mental status changes, sepsis, diarrhea with severe dehydration, and/or physician/nursing clinical assessment that the child needs immediate hospitalization
  • Participation in a separate therapeutic feeding program within the past month
  • Known allergy to study food ingredient (peanut, milk, fish)
  • Clinically evident developmental delay (most often determined based on research nursing assessment of physical appearance, movement, and informal discussion with caregiver)
  • Presence of a chronic severe medical condition (other than tuberculosis and HIV), such as congenital heart disease

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food)

One sachet contains 92g of MFGM-RUTF. During SAM treatment, each participant will be given sufficient MFGM-RUTF to consume 2 sachets per day, which will provide approximately 1000 calories, 27g of protein, 63g of fat, and over 1 RDA of micronutrients.

MFGM whey protein/fat concentrate powder used in place of skim milk powder in peanut paste-based ready-to-use therapeutic food meeting Codex Alimentarius specifications. There will be 10g of MFGM-containing whey protein/fat concentrate powder per 100g of MFGM-RUTF. Other ingredients and amounts per 100g: 9.5g rice flour, 5g whey permeate, 18.5g palm oil, 31g peanut paste, 22.1g sugar, 2.9g micronutrient mix, 1g fish oil.

Oral amoxicillin tablets twice per day for 7 days dosed based on weight

Malaria chemoprophylaxis, dosed by weight, to be given every month during SAM treatment

Comparador Ativo: S-RUTF (standard ready-to-use therapeutic food)

One sachet contains 92g of S-RUTF. During SAM treatment, each participant will be given sufficient S-RUTF to consume 2 sachets per day, which will provide approximately 1000 calories, 27g of protein, 60g of fat, and over 1 RDA of micronutrients.

Oral amoxicillin tablets twice per day for 7 days dosed based on weight

Malaria chemoprophylaxis, dosed by weight, to be given every month during SAM treatment

Standard peanut paste-based ready-to-use therapeutic food made with skim milk powder meeting Codex Alimentarius specifications. This RUTF is modeled on the most widely used recipe worldwide, containing per 100g: 19.5g skim milk powder, 9.3g palm oil, 7g canola oil, 31.3g peanut paste, 28g sugar, 1g soy flakes, 1g hydrogenated vegetable oil, and 2.9g micronutrient mix.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Malawi Developmental Assessment Tool global z-score
Prazo: 6 (5-7) months after SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

6 (5-7) months after SAM treatment completion
Composite of poor severe acute malnutrition treatment outcomes
Prazo: 2-12 weeks of therapeutic feeding

This composite outcome will include death, hospitalization, and remaining severely malnourished despite 12 weeks of treatment

2-12 weeks of therapeutic feeding

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Malawi Developmental Assessment Tool gross motor domain z-score
Prazo: 6 (5-7) months after SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

6 (5-7) months after SAM treatment completion
Malawi Developmental Assessment Tool fine motor domain z-score
Prazo: 6 (5-7) months after SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

6 (5-7) months after SAM treatment completion
Malawi Developmental Assessment Tool language domain z-score
Prazo: 6 (5-7) months after SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

6 (5-7) months after SAM treatment completion
Malawi Developmental Assessment Tool social-emotional domain z-score
Prazo: 6 (5-7) months after SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

6 (5-7) months after SAM treatment completion
Remaining severely malnourished at end of SAM treatment
Prazo: 12 weeks of therapeutic feeding

For MUAC enrollment: MUAC < 11.5 cm For WLZ enrollment: WLZ < -3 For enrollment by both MUAC and WLZ: either remaining in SAM range For nutritional edema enrollment: continued edema

12 weeks of therapeutic feeding
Death during SAM treatment
Prazo: 2-12 weeks of therapeutic feeding

As per caregiver/family report

2-12 weeks of therapeutic feeding
Hospitalization during SAM treatment
Prazo: 2-12 weeks of therapeutic feeding

Participant determined to require hospitalization. Determination may be made by caregiver/family, government health workers, or may be recommended by trial staff for clinical decompensation.

2-12 weeks of therapeutic feeding
Graduation from SAM treatment
Prazo: 2-12 weeks of therapeutic feeding

For MUAC enrollment: MUAC ≥ 12.5cm For WLZ enrollment: WLZ > -2 based on enrollment length For MUAC and WLZ enrollment: may meet either For edema enrollment: resolution of edema, with at least 4 weeks treatment

2-12 weeks of therapeutic feeding
Malawi Developmental Assessment Tool global z-score
Prazo: Within 1 month of SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool gross motor domain z-score
Prazo: Within 1 month of SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool fine motor domain z-score
Prazo: Within 1 month of SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool language domain z-score
Prazo: Within 1 month of SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool social-emotional domain z-score
Prazo: Within 1 month of SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better

Within 1 month of SAM treatment completion
Rate of weight change
Prazo: Across initial 4 weeks of therapeutic feeding, or 2 weeks if graduate after 2 weeks

g / kg / day

Across initial 4 weeks of therapeutic feeding, or 2 weeks if graduate after 2 weeks
Rate of length change
Prazo: Across 2-12 weeks of therapeutic feeding

mm / week

Across 2-12 weeks of therapeutic feeding
Rate of mid-upper arm circumference change
Prazo: Across 2-12 weeks of therapeutic feeding

mm / week

Across 2-12 weeks of therapeutic feeding
Rate of change in length-for-age z-score across entire follow-up
Prazo: 7-10 months (2-12 weeks of therapeutic feeding, 5-7 months of follow-up thereafter)

Difference in LAZ at final visit and initial visit divided by time months transpired

7-10 months (2-12 weeks of therapeutic feeding, 5-7 months of follow-up thereafter)
Diarrhea incidence during SAM treatment
Prazo: 2-12 weeks of therapeutic feeding

Caregiver report of participant diarrhea (>2 loose stools per day) during SAM treatment

2-12 weeks of therapeutic feeding
Fever incidence during SAM treatment
Prazo: 2-12 weeks of therapeutic feeding

Caregiver report of participant fever during SAM treatment

2-12 weeks of therapeutic feeding
Plasma DHA status at end of SAM treatment
Prazo: Collected after 2-12 weeks of therapeutic feeding

Blood spot DHA % total fatty acids in subset of participants at end of therapeutic feeding

Collected after 2-12 weeks of therapeutic feeding
Fecal host mRNA transcripts as markers of environmental enteric dysfunction at end of SAM treatment
Prazo: Collected after 2-12 weeks of therapeutic feeding

CD53, CDX1, HLA-DRA, TNF, S100A8, MUC12, and REG1A

Collected after 2-12 weeks of therapeutic feeding
Malawi Developmental Assessment Tool global z-score trajectory
Prazo: 6 (5-7) months after SAM treatment completion

Change in MDAT global z-score between initial test and final test

6 (5-7) months after SAM treatment completion

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Malawi Developmental Assessment Tool global z-score in sub-groups
Prazo: 6 (5-7) months after SAM outcome

Age-standardized score, -6 to +6, higher scores are better. Will be tested in subgroups based on SAM treatment outcome (graduation vs. other), age at enrollment, and sex

6 (5-7) months after SAM outcome
Malawi Developmental Assessment Tool global z-score in sub-groups
Prazo: Within 1 month of SAM treatment completion

Age-standardized score, -6 to +6, higher scores are better. Will be tested in subgroups based on SAM treatment outcome (graduation vs. other), age at enrollment, and sex

Within 1 month of SAM treatment completion
Composite of poor severe acute malnutrition treatment outcomes
Prazo: 2-12 weeks of therapeutic feeding

This composite outcome will include death, hospitalization, and remaining severely malnourished despite 12 weeks of treatment. This will be tested in subgroups by age at enrollment, sex, and enrollment criteria.

2-12 weeks of therapeutic feeding

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Mark J Manary, MD, Washington University School of Medicine
  • Investigador principal: Kevin B Stephenson, MD, Washington University School of Medicine
  • Diretor de estudo: Indi Trehan, MD, MPH, University of Washington

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

22 de setembro de 2025

Conclusão Primária (Estimado)

1 de dezembro de 2027

Conclusão do estudo (Estimado)

1 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

5 de março de 2025

Enviado pela primeira vez que atendeu aos critérios de CQ

5 de março de 2025

Primeira postagem (Real)

11 de março de 2025

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de novembro de 2026

Última verificação

1 de outubro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Prazo de Compartilhamento de IPD

Within 12 months of primary publication

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • ANALYTIC_CODE
  • CSR

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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