ZARI: The Efficacy of Zinc-biofortified Rice in Bangladeshi Children

Sponsor
Swiss Federal Institute of Technology (Other)
Overall Status
Completed
CT.gov ID
NCT03079583
Collaborator
HarvestPlus (Other), BRAC University (Other)
520
2
2
12.8
260
20.3

Study Details

Study Description

Brief Summary

To assess the efficacy of the zinc biofortified rice on plasma zinc concentrations in infants from a rural area of Bangladesh.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Intervention-group
  • Dietary Supplement: Control-group
N/A

Detailed Description

Rationale: Around the world and estimated 30% of the population is at risk of Zinc deficiency, mainly due to monotonous plant base diets and the poor bioavailability of this sources. One staple food crop which is low in zinc content is rice. Therefore, zinc deficiency is highly common in Asia. Zinc plays a major role in child growth and neurobehavioral development. Furthermore, it is linked to infection control and normal immune response. One way to add extra zinc to someone's diet is zinc bio fortification of staple crops, which can be a cost saving sustainable approach to improve zinc nutrition. However, data on long-term intake of biofortified crops with zinc is scarce and efficacy of newly developed rice crops high in zinc are not well known.

Objective: The objective is to assess the efficacy of a newly developed zinc biofortified rice variety on plasma zinc concentrations in children in a rural area of Bangladesh when compared to their controls in a 9 month randomized controlled trial (RCT).

Study design: A double randomized control trial. Study population: Stunted children whom are zinc deficient at start of the study intervention determined by plasma zinc levels <9.9 µmol/L.

Main study parameters/endpoints: The difference in zinc status between the intervention and control group expressed in blood plasma zinc levels. Plasma zinc will be measured 4 times during the intervention period. Besides plasma zinc other zinc biomarkers will be tested for their usefulness.

Study Design

Study Type:
Interventional
Actual Enrollment :
520 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
The Efficacy of Zinc-biofortified Rice in Improving Zinc Status in Young Bangladeshi Children, a Double Blind Randomized Controlled Trial
Actual Study Start Date :
Apr 1, 2018
Actual Primary Completion Date :
Apr 25, 2019
Actual Study Completion Date :
Apr 25, 2019

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Control-group

Control Rice used for meal, normal zinc level

Dietary Supplement: Control-group
Control Rice with normal zinc levels

Active Comparator: Intervention-group

Biofortified Rice used for meal, around 30% higher zinc level

Dietary Supplement: Intervention-group
Biofortified Rice is grown by foliar Zn application

Outcome Measures

Primary Outcome Measures

  1. plasma zinc [4 collection points in total. 2 fixed at start and end of intervention (week 1&36, T=1,4). 2 sparse random sampling points (RSP) in-between T=1-4. First RSP between 2-5 months (week 5-20 T=2). Second RSP between 5-8 months (week 21-32,T=3).]

    Change of plasma zinc values from baseline to endpoint and 2 times within study period

Secondary Outcome Measures

  1. Inflammatory markers [4 collection points in total. 2 fixed at start and end of intervention (week 1&36, T=1,4). 2 sparse random sampling points (RSP) in-between T=1-4. First RSP between 2-5 months (week 5-20 T=2). Second RSP between 5-8 months (week 21-32,T=3).]

    C reactive protein (CRP),alpha1-acid glycoprotein (AGP)

  2. Length [4 collection points in total. 2 fixed at start and end of intervention (week 1&36, T=1,4). 2 sparse random sampling points (RSP) in-between T=1-4. First RSP between 2-5 months (week 5-20 T=2). Second RSP between 5-8 months (week 21-32,T=3).]

    Length (in cm) measurement for anthropometric (HAZ-scores).

  3. Weight [4 collection points in total. 2 fixed at start and end of intervention (week 1&36, T=1,4). 2 sparse random sampling points (RSP) in-between T=1-4. First RSP between 2-5 months (week 5-20 T=2). Second RSP between 5-8 months (week 21-32,T=3).]

    Weight (in kg) measurement for anthropometric (HAZ-scores).

  4. Morbidity [Fixed assessment once a week for every participant throughout the intervention period (week 1-36).]

    diarrhea and disease episodes will be recorded weekly throughout the study

  5. FADS analyses [Secondary analyses of collected plasma samples, in subset of participants (75 children from each group, random selected, matched baseline and endpoint samples)]

    FADS plasma analyses for zinc biomarker determination

  6. Iron status [4 collection points in total. 2 fixed at start and end of intervention (week 1&36, T=1,4). 2 sparse random sampling points (RSP) in-between T=1-4. First RSP between 2-5 months (week 5-20 T=2). Second RSP between 5-8 months (week 21-32,T=3).]

    Plasma ferritin

  7. Iron status [4 collection points in total. 2 fixed at start and end of intervention (week 1&36, T=1,4). 2 sparse random sampling points (RSP) in-between T=1-4. First RSP between 2-5 months (week 5-20 T=2). Second RSP between 5-8 months (week 21-32,T=3).]

    Hemoglobin

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Months to 36 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 12-36 months of age (at baseline assessment)

  • Low plasma Zn concentration (<10.71 µmol/L)

  • Marginally stunted (height for age Z-score <-1.75)

  • The informed consent form has been read and signed by the caregiver (or has been read out to the caregiver in case of illiteracy)

Exclusion Criteria:
  • Severe Anemia (Hb< 70 g/L)

  • Chronic or acute illness or other conditions that in the opinion of the Principle Investigator (PI) or co-researchers would affect Zn metabolism or would render the participant unable to comply with the protocol (based on self-reporting or diagnosed during screening)

  • Participants taking part in other studies requiring the drawing of blood

  • Not planning long-term residence in study site

  • Regular intake (>2 days) of iron-containing mineral and vitamin supplements or fortified foods within the last 2 months

  • Chronic use of drugs that affect the metabolism of Zn, including reducing absorption or increasing excretion; e.g., tuberculosis medications (ethambutal and isoniazides), drugs used as treatment for entamoeba hystolica (diiodohydroxyquin), drugs that reduce stomach acidity (H2 blockers and proton pump inhibitory), antidepressants (nialamide and socarboxazid), anti-inflammatory drugs (corticosteroids), diuretics (thiazides).

Contacts and Locations

Locations

Site City State Country Postal Code
1 BRACU, Bangladesh Dhaka Bangladesh
2 Swiss Federal Institute of Technology (ETH) Zurich Switzerland 8092

Sponsors and Collaborators

  • Swiss Federal Institute of Technology
  • HarvestPlus
  • BRAC University

Investigators

  • Principal Investigator: Michael B Zimmermann, Prof. Dr., Professor, Laboratory of Human Nutrition, Department of health science and technology, ETH Zurich, Zurich, Switzerland
  • Principal Investigator: Malay K Mridha, Assoc. Prof., Associate Professor, James P Grant school of Public Health, BRAC University, Dhaka, Bangladesh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Swiss Federal Institute of Technology
ClinicalTrials.gov Identifier:
NCT03079583
Other Study ID Numbers:
  • ZARI_1_trail
First Posted:
Mar 14, 2017
Last Update Posted:
Jul 22, 2021
Last Verified:
Jul 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Swiss Federal Institute of Technology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2021