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- Ensaio Clínico NCT06869850
Rutf aprimorado pela membrana de gordura do leite para crianças com desnutrição aguda grave (MEND-SAM)
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
Status
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
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
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
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
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
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
Patrocinador
Colaboradores
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
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Transtornos Mentais, Desordem Mental
- Distúrbios Nutricionais
- Peso corporal
- Alterações de Peso Corporal
- Distúrbios Neurocognitivos
- Distúrbios Cognitivos
- Desnutrição
- Perda de peso
- Magreza
- Condições Patológicas, Sinais e Sintomas
- Doenças Nutricionais e Metabólicas
- Sinais e sintomas
- Desnutrição Aguda Grave
- Disfunção cognitiva
- Caquexia
- Kwashiorkor
- Compostos de enxofre
- Produtos químicos orgânicos
- Compostos heterocíclicos, 1 anel
- Compostos heterocíclicos
- Compostos heterocíclicos, 2 anel
- Compostos heterocíclicos, anel fundido
- Hidrocarbonetos
- Hidrocarbonetos, cíclicos
- Hidrocarbonetos, aromáticos
- Amidas
- Compostos de anilina
- Aminas
- Pirimidinas
- Derivados de benzeno
- Penicilina g
- beta-lactamas
- Lactamas
- Benzenésulfonamidas
- Sulfonamidas
- Sulfanilamidas
- Sulfonas
- Ampicilina
- Penicilins
- Amoxicilina
- Pirimetamina
- Sulfadoxina
Outros números de identificação do estudo
- 202503015
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
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
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