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Early Life Interventions for Childhood Growth and Development In Tanzania (ELICIT)

Primary Purpose

Malnutrition, Stunting, Cognitive Development

Status
Completed
Phase
Phase 2
Locations
Tanzania
Study Type
Interventional
Intervention
Azithromycin Oral Liquid Product
Nitazoxanide Oral Suspension
Nicotinamide
Placebos
Sponsored by
Haydom Lutheran Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition

Eligibility Criteria

0 Days - 14 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Maternal age ≥18
  2. Infant ≤ 14 days

Exclusion Criteria:

  1. Maternal inability to adhere to protocol
  2. Multiple gestation
  3. Severe illness (significant birth defect, hospitalization, severe neonatal illness)
  4. Birth weight <1500 g
  5. Lack of breastfeeding at enrollment (and lack of intention to continue breastfeeding at time of enrollment).

Sites / Locations

  • Haydom Lutheran Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

Nicotinamide and Antimicrobials

Antimicrobials only

Nicotinamide only

No active treatment

Arm Description

Nicotinamide Azithromycin Oral Liquid Product Nitazoxanide Oral Suspension

Placebo Azithromycin Oral Liquid Product Nitazoxanide Oral Suspension

Nicotinamide Placebo Placebo

Placebo Placebo Placebo

Outcomes

Primary Outcome Measures

Height-for-age z-score (HAZ) at 18 months

Secondary Outcome Measures

Weight-for-age z-score (WAZ) at 18 months
Head circumference-for-age z-score (HCAZ) at 18 months
Stunting
HAZ <-2
All cause mortality
Hospitalization
Childhood illness
Incidence of diarrhea, lower respiratory infection and febrile illness
Anemia
Moderate to severe anemia by WHO definition for age and altitude
Enteropathogen burden
Microbiota composition
Composition of intestinal microbiome
Stool myeloperoxidase concentration
Stool myeloperoxidase ELISA
C-reactive protein concentration in serum
High-sensitivity CRP concentration
Insulin-like growth factor 1 concentration in serum
Collagen X concentration in serum
Tryptophan-kynurenine ratio
Ratio of tryptophan concentration to kynurenine concentration in metabolomic testing
Niacin and nicotinamide metabolite concentration
Concentration of downstream metabolites of niacin and nicotinamide as tested by metabolomic analysis
Small intestinal bacterial overgrowth
Prevalence of SIBO as tested via exhaled hydrogen
Malawi Developmental Assessment Tool score
The MDAT is a measure of child cognitive development

Full Information

First Posted
August 29, 2017
Last Updated
May 5, 2021
Sponsor
Haydom Lutheran Hospital
Collaborators
University of Virginia, Bill and Melinda Gates Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03268902
Brief Title
Early Life Interventions for Childhood Growth and Development In Tanzania
Acronym
ELICIT
Official Title
Early Life Interventions for Childhood Growth and Development In Tanzania
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
September 5, 2017 (Actual)
Primary Completion Date
February 28, 2020 (Actual)
Study Completion Date
March 26, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Haydom Lutheran Hospital
Collaborators
University of Virginia, Bill and Melinda Gates Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to assess growth and cognitive effects of treatment with azithromycin and nitazoxanide and/or nicotinamide (vitamin B3) supplementation nicotinamide.
Detailed Description
Children living in rural sub-Saharan Africa experience massive challenges to child thriving, with poor linear growth and delays in child development. In a cohort of 211 children living in the rural Haydom area of Tanzania (participating in the Interactions of Malnutrition & Enteric Infections: Consequences for Child Health and Development "MAL-ED" Study), 70.6% had stunted growth at 18 months. This rate of moderate and severe stunting (length-for-age z-score [HAZ] <-2 standard deviations) was the highest of the 8 study sites in MAL-ED. This enormous deficit is likely associated with high rates of enteric infections with Campylobacter, E. coli pathotypes, Cryptosporidium, and Giardia, organisms susceptible to azithromycin and/or nitazoxanide. Infections such as these occur frequently in developing areas and are often associated with environmental enteropathy, including ongoing enteric inflammation and loss of enterocyte integrity, leading to possible bacterial translocation and poorer absorption of ingested nutrients. The consequences of these infections, enteric dysfunction and poor nutrient absorption frequently include growth stunting, learning delays, and an overall loss of human capital. Emerging evidence suggests a potential role for the tryptophan-niacin pathway (including the end-product nicotinamide, an isoform of vitamin B3) in decreasing mucosal inflammation and affecting enteral microbiota. At the Tanzania site of MAL-ED, serum levels of tryptophan were related to subsequent linear growth, further suggesting importance of the tryptophan-niacin pathway. What is not clear is whether early childhood growth and development could be improved by targeting enteric infection and the tryptophan-niacin pathway by 1) delivering antibiotics against specific bacteria and/or 2) providing vitamin B3 as nicotinamide/niacinamide. The main analysis will be intention-to-treat but a secondary analysis will be per protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition, Stunting, Cognitive Development, Enteric Pathogens

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Factorial Assignment
Model Description
Each intervention will be assigned independently. Intervention domains will be randomized separately on an individual basis. This will provide 4 different combinations of interventions: 1). Nicotinamide, azithromycin and nitazoxanide 2). Azithromycin and nitazoxanide 3). Nicotinamide only 4). No active treatment.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Both participants and investigators will be blinded to the treatments allocated to each participant. The members of the DSMB will also be blinded.
Allocation
Randomized
Enrollment
1188 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nicotinamide and Antimicrobials
Arm Type
Experimental
Arm Description
Nicotinamide Azithromycin Oral Liquid Product Nitazoxanide Oral Suspension
Arm Title
Antimicrobials only
Arm Type
Experimental
Arm Description
Placebo Azithromycin Oral Liquid Product Nitazoxanide Oral Suspension
Arm Title
Nicotinamide only
Arm Type
Experimental
Arm Description
Nicotinamide Placebo Placebo
Arm Title
No active treatment
Arm Type
Placebo Comparator
Arm Description
Placebo Placebo Placebo
Intervention Type
Drug
Intervention Name(s)
Azithromycin Oral Liquid Product
Other Intervention Name(s)
Throza DPS
Intervention Description
Azithromycin 20 mg/kg administered by study personnel at 6, 9, 12 and 15 months
Intervention Type
Drug
Intervention Name(s)
Nitazoxanide Oral Suspension
Other Intervention Name(s)
Alinia
Intervention Description
Nitazoxanide 100 mg given twice daily for 3 days at 12 and 15 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Nicotinamide
Other Intervention Name(s)
Vitamin B3
Intervention Description
Mothers in the nicotinamide arm will be given nicotinamide 250 mg daily from delivery through 6 months post-partum in capsule form. Children in the nicotinamide arm will be given 100 mg/d in powder form between 6 and 18 months of age
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
Contain inert excipients only. Azithromycin placebo 20 mg/kg administered by study personnel at 6, 9, 12 and 15 months. Nitazoxanide placebo 100 mg given twice daily for 3 days at 12 and 15 months. Mothers in the nicotinamide placebo arm will be given placebo 250 mg daily from delivery through 6 months post-partum in capsule form. Children in the nicotinamide placebo arm will be given 100 mg/d of placebo in powder form between 6 and 18 months of age
Primary Outcome Measure Information:
Title
Height-for-age z-score (HAZ) at 18 months
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Weight-for-age z-score (WAZ) at 18 months
Time Frame
18 months
Title
Head circumference-for-age z-score (HCAZ) at 18 months
Time Frame
18 months
Title
Stunting
Description
HAZ <-2
Time Frame
18 months
Title
All cause mortality
Time Frame
0-18 months
Title
Hospitalization
Time Frame
0-18 months
Title
Childhood illness
Description
Incidence of diarrhea, lower respiratory infection and febrile illness
Time Frame
0-18 months
Title
Anemia
Description
Moderate to severe anemia by WHO definition for age and altitude
Time Frame
12 and 18 months
Title
Enteropathogen burden
Time Frame
6, 6.5, 12, 12.5, 18 months
Title
Microbiota composition
Description
Composition of intestinal microbiome
Time Frame
6, 6.5, 12, 18 months
Title
Stool myeloperoxidase concentration
Description
Stool myeloperoxidase ELISA
Time Frame
6, 12, 18 months
Title
C-reactive protein concentration in serum
Description
High-sensitivity CRP concentration
Time Frame
12 and 18 months
Title
Insulin-like growth factor 1 concentration in serum
Time Frame
12 and 18 months
Title
Collagen X concentration in serum
Time Frame
12 and 18 months
Title
Tryptophan-kynurenine ratio
Description
Ratio of tryptophan concentration to kynurenine concentration in metabolomic testing
Time Frame
12 and 18 months
Title
Niacin and nicotinamide metabolite concentration
Description
Concentration of downstream metabolites of niacin and nicotinamide as tested by metabolomic analysis
Time Frame
6, 12, 18 months
Title
Small intestinal bacterial overgrowth
Description
Prevalence of SIBO as tested via exhaled hydrogen
Time Frame
6, 12 and 18 months
Title
Malawi Developmental Assessment Tool score
Description
The MDAT is a measure of child cognitive development
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Days
Maximum Age & Unit of Time
14 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Maternal age ≥18 Infant ≤ 14 days Exclusion Criteria: Maternal inability to adhere to protocol Multiple gestation Severe illness (significant birth defect, hospitalization, severe neonatal illness) Birth weight <1500 g Lack of breastfeeding at enrollment (and lack of intention to continue breastfeeding at time of enrollment).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Estomih Mduma
Organizational Affiliation
Haydom Lutheran Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haydom Lutheran Hospital
City
Haydom
State/Province
Manyara
Country
Tanzania

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34582462
Citation
DeBoer MD, Platts-Mills JA, Elwood SE, Scharf RJ, McDermid JM, Wanjuhi AW, Jatosh S, Katengu S, Parpia TC, Rogawski McQuade ET, Gratz J, Svensen E, Swann JR, Donowitz JR, Mdoe P, Kivuyo S, Houpt ER, Mduma E. Effect of scheduled antimicrobial and nicotinamide treatment on linear growth in children in rural Tanzania: A factorial randomized, double-blind, placebo-controlled trial. PLoS Med. 2021 Sep 28;18(9):e1003617. doi: 10.1371/journal.pmed.1003617. eCollection 2021 Sep.
Results Reference
derived
PubMed Identifier
29982218
Citation
DeBoer MD, Platts-Mills JA, Scharf RJ, McDermid JM, Wanjuhi AW, Gratz J, Svensen E, Swann JR, Donowitz JR, Jatosh S, Houpt ER, Mduma E. Early Life Interventions for Childhood Growth and Development in Tanzania (ELICIT): a protocol for a randomised factorial, double-blind, placebo-controlled trial of azithromycin, nitazoxanide and nicotinamide. BMJ Open. 2018 Jul 7;8(7):e021817. doi: 10.1136/bmjopen-2018-021817.
Results Reference
derived

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Early Life Interventions for Childhood Growth and Development In Tanzania

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