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Hypoallergenic and Anti-inflammatory Feeds in Malawian Children With Severe Acute Malnutrition (SAM)

Hypoallergenic and Anti-inflammatory Feeds to Treat Intestinal Inflammation in Malawian Children With Severe Acute Malnutrition: A Pilot Randomized Controlled Clinical Trial (SAM)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02639416
Acronym
SAM
Enrollment
95
Registered
2015-12-24
Start date
2016-01-01
Completion date
2017-01-11
Last updated
2021-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Enteritis, Severe Malnutrition

Keywords

severe acute malnutrition, polymeric therapeutic formula, elemental therapeutic formula

Brief summary

Children with complicated severe acute malnutrition (SAM), such as inability to take adequate feeds, infection and diarrhoea, require in-patient management. Despite following a well-established World Health Organisation (WHO) protocol, outcomes are poor. Case fatality often exceeds 20%. Amongst survivors discharged home, many subsequently die, have long-term poor growth or recurrence of SAM. It has long been recognized that children with SAM have intestinal inflammation and that this persists despite management according to WHO guidelines. The inflammation is thought to result from increased exposure to microbial pathogens in the gut in areas with poor sanitation. The damaged lining of the intestine impairs food digestion and absorption, likely allows gut bacteria to enter the blood stream to cause sepsis and also exposes the gut immune cells to microbial and food antigens causing the inflammation to persist. Failure to treat the intestinal inflammation is likely to contribute to the poor response to treatment and poor long-term outcomes in many children with SAM. The intestinal inflammation seen in SAM is very similar to that which occurs in food intolerance (e.g. intolerance to cow's milk protein) and inflammatory bowel disease. In these conditions, the inflammation is treated very effectively with hypoallergenic (elemental) and anti-inflammatory (polymeric) formulas. These are nutritionally complete feeds that have a similar composition to the feeds used for nutritional rehabilitation in SAM. We aim to undertake a pilot study to see if an elemental and/or polymeric formula are tolerated by children with SAM and help to reduce intestinal inflammation. We also aim to learn more about the intestinal inflammation in general that occurs in SAM by observing carefully the effect of these specific formulae and to do in-depth metabolic analyses.

Detailed description

We will study children admitted to the Moyo ward at the Queen Elizabeth Central Hospital, Blantyre, Malawi with complicated SAM. Following informed consent, children will be recruited once they have completed the initial stabilisation phase of management and enter the transition phase to nutritional rehabilitation. They will be randomly allocated to one of 3 arms, either 1) standard feeds (F-100 and/or ready-to-use therapeutic feeds), 2) a polymeric therapeutic formula or 3) an elemental therapeutic formula. The alternative feeds will be supplemented with micronutrients to be equivalent in composition to F-100. All children will remain admitted to the ward for 2 weeks and receive exclusively the allocated formula. All other aspects of the management of SAM will follow current practice based on WHO guidelines.

Interventions

DIETARY_SUPPLEMENTPolymeric formula

Polymeric formulae are recommended in the management of inflammatory bowel disease in children

DIETARY_SUPPLEMENTElemental formula

Elemental formulae are recommended in cow's milk and other food intolerances in children.

Standard management with F-100 and/or RUTF

Sponsors

University of Toronto
CollaboratorOTHER
Kamuzu University of Health Sciences
CollaboratorOTHER
Queen Elizabeth Central Hospital, Blantyre, Malawi
CollaboratorUNKNOWN
Liverpool School of Tropical Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 23 Months
Healthy volunteers
No

Inclusion criteria

* Age 6-23 months * SAM diagnosed according to WHO criteria: (Weight-for-height z score \<-3 and/or mid-upper arm circumference \<11.5 cms and/or nutritional oedema) * Admitted to hospital because of SAM with medical complications or fails an appetite test * Completed stabilization phase and entering the second phase in refeeding; the transition Phase * Willing to stay on the ward for 2 weeks after the stabilization phase (travel expenses will be provided)

Exclusion criteria

* Specific cause of malnutrition (e.g. cerebral palsy, other organ disease) * Sibling admitted with SAM at the same time * Unwilling to stay on ward for at least 2 weeks * Declined to give consent * Participating in another study

Design outcomes

Primary

MeasureTime frameDescription
Change in faecal calprotectin14 daysValidated marker of intestinal inflammation

Secondary

MeasureTime frameDescription
Days with diarrhoea1-14 daysnumber of days with 3 or more loose/watery stools
Weight gain1-14 dayschange in weight in g/kg/day
Episodes of sepsis1-14 daysClinical diagnosis
Death1-14 daysnumber of children who die

Countries

Malawi

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026