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Maitorasva Globule Membraanin parannettu RUTF lapsille, joilla on vaikea akuutti aliravitsemus (MEND-SAM)

sunnuntai 1. marraskuuta 2026 päivittänyt: Washington University School of Medicine

MFGM-parannettu RUTF SAM-lapsille

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

Tutkimuksen yleiskatsaus

Yksityiskohtainen kuvaus

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.

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

1600

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskelupaikat

    • Pujehun
      • Bandajuma, Pujehun, Sierra Leone
        • Bandajuma
      • Bandasuma, Pujehun, Sierra Leone
        • Bandasuma
      • Bendu Malen, Pujehun, Sierra Leone
        • Bendu Malen
      • Gbondapi, Pujehun, Sierra Leone
        • Gbondapi
      • Jendema, Pujehun, Sierra Leone
        • Jendema
      • Potoru, Pujehun, Sierra Leone
        • Potoru
      • Pujehun, Pujehun, Sierra Leone
        • Static
      • Sahn Malen, Pujehun, Sierra Leone
        • Sahn Malen
      • Taninahun, Pujehun, Sierra Leone
        • Taninahun
      • Zimmi, Pujehun, Sierra Leone
        • Zimmi

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

6 kuukautta - 4 vuotta (Lapsi)

Hyväksyy terveitä vapaaehtoisia

Ei

Sukupuolet, jotka voivat opiskella

Kaikki

Kuvaus

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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Kolminkertaistaa

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: 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

Active Comparator: 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.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Malawi Developmental Assessment Tool global z-score
Aikaikkuna: 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
Aikaikkuna: 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

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Malawi Developmental Assessment Tool gross motor domain z-score
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 2-12 weeks of therapeutic feeding

As per caregiver/family report

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

mm / week

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

Muut tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Malawi Developmental Assessment Tool global z-score in sub-groups
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Tutkijat

  • Päätutkija: Mark J Manary, MD, Washington University School of Medicine
  • Päätutkija: Kevin B Stephenson, MD, Washington University School of Medicine
  • Opintojohtaja: Indi Trehan, MD, MPH, University of Washington

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

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Ensimmäinen lähetetty

Keskiviikko 5. maaliskuuta 2025

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Keskiviikko 5. maaliskuuta 2025

Ensimmäinen Lähetetty (Todellinen)

Tiistai 11. maaliskuuta 2025

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Tiistai 3. marraskuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Sunnuntai 1. marraskuuta 2026

Viimeksi vahvistettu

Torstai 1. lokakuuta 2026

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Tähän tutkimukseen liittyvät termit

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

JOO

IPD-jaon aikakehys

Within 12 months of primary publication

IPD-jakamista tukeva tietotyyppi

  • STUDY_PROTOCOL
  • MAHLA
  • ICF
  • ANALYTIC_CODE
  • CSR

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