CClinicalTrials.gg
Status unknownNCT02257762Updated Sep 15, 2016

Efficacy of a Multiple Micronutrient-Fortified Lipid-Based Nutrient Supplement for Children Under Two in Cambodia

An interventional study of LNS and Corn-soy blend ++ (CSB++) in Child Malnutrition, sponsored by Institut de Recherche pour le Developpement, Cambodia. Status unknown at 1 site in Cambodia. Open to participants aged 6 Months to 12 Months, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-15.

Sponsored by Institut de Recherche pour le Developpement, Cambodia · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Sep 2016), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
487
Allocation
Randomized
Ages
6 Months to 12 Months
Sex
All
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Study summary

The purpose of this trial is to evaluate the efficacy of the LNS on children aged 6-17 months in preventing growth faltering and improving micronutrient status. The impact of product will be compared to Corn Soy Blend ++ (CSB++), Sprinkles, and to a control group consuming an unsupplemented diet, which is usually borbor at an early age, and thereafter, family foods.

Read the detailed description

BACKGROUND:

In Cambodia, progress in combatting malnutrition has stalled. In 2010, 40% of all children under five (and 49% of 4-5 year-olds) were stunted, 11% were wasted, and 28% were underweight, indicating, respectively, chronic and acute malnutrition, and a combination of the two. Stunting is partially attributed to poor complementary feeding, which remains inadequate for achieving growth outcomes and micronutrient status.

Malnutrition can be prevented with supplementary foods. These foods usually contain a source of protein and lipids such as powered milk, soy or peanuts, and multiple micronutrients. They can be prepared as a fortified blended product, such as Corn-Soy Blend++ (CSB++), that is mixed with water to make a porridge, or ready-to-use supplementary foods (RUSFs). The latter are usually lipid-based nutrient supplements (LNSs) which are often pastes such as the peanut-based Plumpy'Nut™. These energy-dense supplementary foods contain both macro and micronutrients and are used to prevent and treat moderate acute malnutrition by promoting improved linear growth, weight gain and micronutrient status among children. Until recently, treatment of moderate acute malnutrition has relied on fortified blended products. The new RUSFs are also proving effective, as they are higher energy and have a longer shelf life, and since they require no preparation, are convenient. Another common nutrition intervention is multiple micronutrient supplements such as Sprinkles. These are individually-packed powders that can be added to food. However, micronutrients are more likely to achieve growth outcomes when they are combined with energy, for example, in lipid-based nutrient supplements and there is no evidence that micronutrient powders alone contribute to growth.

Until June 2014, the United Nations World Food Program (WFP) used CSB++ (now called Supercereal Plus) to treat and prevent moderate acute malnutrition in Cambodia. Sprinkles are also being distributed, though not widely, to prevent micronutrient deficiencies. These products that have been recently or are currently used are relatively expensive to procure and ship to Cambodia and in the case of Sprinkles, are not as effective as foods that contain macronutrients. Moreover, CSB++ was not very well accepted in practice, and WFP has phased it out. Therefore, UNICEF and the Cambodian Ministry of Health are looking for a locally-produced product containing macro and micronutrients to prevent growth faltering and improve micronutrient status in Cambodian children.

TRIAL DESIGN AND METHODOLOGY:

Therefore, this trial will evaluate the efficacy of the LNS on children aged 6-17 months in preventing growth faltering and improving micronutrient statu. The impact of product will be compared to CSB++, Sprinkles, and to a control group.

The trial is a prospective, cluster randomised, non-blinded controlled trial among infants 6-17 months of age. The trial aims to establish the superiority of the novel LNS, using CSB++ and Sprinkles as active comparators and the unimproved diet as a control. The allocation ratio is 1:1. The study will take place over 8 months.

The study will be conducted in 28 sites in peri-urban Phnom Penh. Infants aged 6-12 months will be recruited. Upon consent and enrolment, baseline data will be collected from the participants. This will include demographics, morbidity, anthropometry (weight, height, mid-upper arm circumference, skinfolds), haematological and stool samples, dietary data (breastfeeding, food frequency and dietary diversity). Data will be collected monthly, and haematological samples will be collected again at endline.

Participants will then be provided with a one month supply of the food to which their site has been allocated. Staff will explain how to prepare the food, how often it should be consumed, and who should consume it (i.e. subjects). Participants will be provided with food on a monthly basis. They will continue to consume the food over a six-month period, at which time endline data, including haematological samples, will be collected.

02

Conditions studied

  • Child Malnutrition

Keywords

  • Ready-to-use supplementary food (RUSF)
  • Lipid-based nutrient supplement (LNS)
  • Multiple micronutrients (MMN)
  • Complementary feeding
  • Home fortification
  • Efficacy/impact
  • Infant and young child feeding (IYCF)
  • Cambodia
  • Cluster randomised controlled trial
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In context

Malnutrition

1,587 studies on the registry are indexed under Malnutrition; 237 are open to participants now.

This study's enrollment of 487 is above the median of 90 across 1,134 interventional studies indexed under Malnutrition.

Browse Malnutrition studies →

Lead sponsor

Institut de Recherche pour le Developpement, Cambodia is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 12 Months
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Children aged 6-12 months
  • Normally nourished or only moderately malnourished (MUAC>115mm, WHZ score>-3)
  • Have not received therapy for acute malnutrition within one month prior to presentation
  • Healthy (no ill-health in past two weeks)
  • Anaemia status - normal, mild or moderate
  • No known food intolerances
  • Informed signed consent of caregiver
  • Caregivers are healthy

Exclusion criteria

Exclusion Criteria:

  • Children \<6 months or >12mths
  • Severely malnourished (MUAC\< 115mm, WHZ score\<3, bipedal pitting oedema).
  • Have received therapy for acute malnutrition within one month prior to presentation
  • Any medical complications at the recruitment time or illness requiring referral or clinic visit in past 2 weeks
  • Severe anaemia (Hb\<70g/l)
  • Known intolerances
  • No informed signed consent of caregiver
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
487 participants (actual)

Study arms

  • Experimental
    Lipid-based nutrient supplement (LNS)

    LNS added to borbor, eaten over 6 months, age 6-12 months to age 11-17 months

    Dietary Supplement: LNS

  • Active comparator
    Corn-soy blend ++ (CSB++)

    CSB++ porridge, eaten over 6 months, age 6-12 months to age 11-17 months

    Dietary Supplement: Corn-soy blend ++ (CSB++)

  • Active comparator
    Sprinkles

    Sprinkles added to borbor, eaten over 6 months, age 6-12 months to age 11-17 months

    Dietary Supplement: Sprinkles

  • No intervention
    Control

    Plain borbor and thereafter family foods, eaten over 6 months, age 6-12 months to age 11-17 months

Interventions

  • Dietary supplementLNS

    Compact, paste-filled wafer snack containing fish, rice, soy, mungbeans, oil, sugar and multiple micronutrients

  • Dietary supplementCorn-soy blend ++ (CSB++)

    Blended flour containing soy, corn, milk powder, oil, sugar and multiple micronutrients.

    Also known as: Supercereal Plus

  • Dietary supplementSprinkles

    Multiple micronutrient powder packaged in sachet.

06

What researchers measure

Primary outcomes

  1. Nutritional status

    Weight-for-height (WHZ), length/height-for-age (L/HAZ), and weight-for-age (WAZ) calculated through monthly weight and height measurements

    Time frame: 6 months

Secondary outcomes

  1. Body composition

    Triceps, biceps and/or subscapular skinfolds

    Time frame: 6 months

  2. Iron status

    Analysis of haemoglobin (g/l), ferritin (µg/l), tranferrin receptor (mg/l), C reactive protein (mg/l), and alpha-1-acid glycoprotein (mg/l)

    Time frame: 6 months

07

Study locations

1 site
  • IRD Cambodia
    Phnom Penh, Cambodia
08

References and documents

Publications

  • Borg B, Sok D, Mihrshahi S, Griffin M, Chamnan C, Berger J, Laillou A, Roos N, Wieringa FT. Effectiveness of a locally produced ready-to-use supplementary food in preventing growth faltering for children under 2 years in Cambodia: a cluster randomised controlled trial. Matern Child Nutr. 2020 Jan;16(1):e12896. doi: 10.1111/mcn.12896. PubMed 31885221 ↗
  • Borg B, Mihrshahi S, Griffin M, Sok D, Chhoun C, Laillou A, Berger J, Wieringa FT. Randomised controlled trial to test the effectiveness of a locally-produced ready-to-use supplementary food (RUSF) in preventing growth faltering and improving micronutrient status for children under two years in Cambodia: a study protocol. Nutr J. 2018 Mar 16;17(1):39. doi: 10.1186/s12937-018-0346-x. PubMed 29548287 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02257762
Lead sponsor
Institut de Recherche pour le Developpement, Cambodia
Collaborators
UNICEF, Department of Fisheries Post-harvest Technologies and Quality Control
Responsible party
Bindi Borg (PhD Candidate, University of Sydney) — Principal investigator
First posted
Oct 6, 2014
Start date
Feb 2016
Primary completion
Oct 2016 (estimated)
Completion
Oct 2016 (estimated)
Last update
Sep 15, 2016

Study contacts

Frank T Wieringa, MD, PhD
study director · IRD
Bindi Borg, MA,PhD cand.
principal investigator · University of Sydney

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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