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Reducing short and long-term consequences of early stunted growth

Reducing short and long-term consequences of early stunted growth. MAGNUS 2 – Milk affecting growth, cognition and the gut in child stunting

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN61878528
Enrollment
850
Registered
2025-07-29
Start date
2025-09-25
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Childhood stunting Musculoskeletal Diseases

Interventions

Children with early stunting who participated in the MAGNUS 1 trial will be invited for a 1-day follow-up at the same health facility as they attended in MAGNUS 1. We expect to be able to relocate up

Sponsors

University of Copenhagen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for children who participated in the MAGNUS 1 trial: 1. Confirmed participation in MAGNUS 1* 2. Living within the catchment area 3. Written informed consent given by parent/caregiver *Confirmed by birth certificate, identity card, or similar documents and/or other confirmation of previous participation in the MAGNUS 1 trial (e.g. informed consent form) Inclusion criteria for the reference group: 1. Age 6-10 years 2. Height-age-z-scores >-1 according to the WHO growth standards 3. Living within the catchment area of MAGNUS 1 trial participants 4. Written informed consent given by parent/caregiver

Exclusion criteria

Exclusion criteria: Exclusion criteria for children who participated in MAGNUS 1 trial and the reference group: 1. SAM; measured as BMI-for-age z-score < -3 OR bilateral pitting oedema 2. Medical complications requiring hospitalization 3. Disability that makes height assessment problematic 4. Participation in another study or program which impacts on this study

Design outcomes

Primary

MeasureTime frame
Cardiometabolic risk markers: 1. Glucose , mmol/L (full blood, HemoCue 201) and HbA1c, mmol/mol (full blood, HemoCue501) 2. Insulin, pmol/L (serum, Cobas 400 immunoassay) 3. Lipids (total cholesterol, mmol/L, high density lipoprotein (HDL) cholesterol, mmol/L and low density lipoprotein (LDL) cholesterol, mmol/L and triglycerides, mmol/L) (serum, Pentra400, Horiba ABX) 4. Blood pressure, mmHg (Welch Allyn ProBP2000) 5. C-peptide, ng/mL (serum, Cobas 400 immunoassay) All primary and secondary outcomes will be measured once. For children who participated in the MAGNUS trial, this corresponds to a 5-year follow-up. For new reference children, this is their first and only assessment.

Secondary

MeasureTime frame
1. Weight, kg (Seca scale) 2. Total height, cm (Shorr height board) 3. Knee-heel length, mm (Shorr knee-height caliper) 4. BMI-for-age z-scores (BAZ) (WHO Anthro) 5. Height-for-age z-scores (HAZ) (WHO Anthro) 6. Child development: 6.1. Cognition test (Kaufman assessment battery for children, KABC-II) 6.2. School achievement (school grades) 6.3. Motor function (grip strength, broad jump) (Takei, Japan and non-elastic measuring tape) 7. Haemoglobin, g/dL (full blood, HemoCue801) 8. Body composition measured by bioelectrical impedance: FM, kg, FFM, kg, FMI, kg/m2, FFMI, kg/m2 (BodyStat 500) 9. Organ size (liver, kidneys and spleen) (ultrasound, Sonoscape) 10. Skin folds: triceps, subscapularis, mm (Harpenden caliper) 11. Waist circumference, cm (non-elastic measuring tape) 12. Abdominal fat (ultrasound, Sonoscape) 13. Mid-upper arm circumference (MUAC), cm (non-elastic measuring tape) 14. Blood hormone markers: 14.1. Insulin-like Growth Factor-1 (IGF-1), ng/mL (serum, Cobas 400 immunoassay) 15. Blood markers of systemic inflammation 15.1. C-reactive protein (CRP), mg/L (serum, high throughput ELISA) 15.2. Alpha-1-acid glycoprotein (AGP), µg/mL (serum, high throughput ELISA) 16. Blood markers of micronutrient status: 16.1. Iron: serum ferritin, µg/L and soluble transferrin receptor, mg/L (serum, high throughput ELISA) 16.2. Vitamin B12: plasma cobalamin, pmol/L (Advia Centaur CP Immunoassay System) and plasma methyl malonic acid (MMA), µmol/L (plasma, mass spectrometry) 16.3. Folate, nmol/L (plasma, Advia Centaur CP Immunoassay System) 16.4. Vitamin A (retinol binding protein), µmol/L (serum, high throughput ELISA) 17. Gut microbiota (stool, 16S rRNA sequencing) 18. Gut function (e.g., plasma citrulline [mass spectrometry], faecal myeloperoxidase, faecal neopterin, faecal alpha-1-antritrypsin [stool, ELISA]) 19. Morbidity (questionnaire) All primary and secondary outcomes will be measured once. For children who participated in the MAGNUS trial, this corresponds to a

Countries

Uganda

Contacts

Public ContactBenedikte Grenov
bgr@nexs.ku.dk+45 (0)20456654

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Aug 25, 2026