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Environmental EnteropathyPhase 2EMPNCT05608928

Ability of the Probiotic Vivomixx to Improve Environmental Enteropathy in Pregnant Women: a Proof of Concept Trial in Bangladesh, Pakistan, Senegal and Zambia

A Phase 2 study testing VSL#3 and Capscan device in people with Environmental Enteropathy, run by Tropical Gastroenterology & Nutrition Group (TROPGAN) at 4 sites in 4 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This trial will determine if a well-established probiotic, Vivomixx, can modulate the maternal microbiota and ameliorate the maternal environmental enteropathy which compromises growth in the first 1000 days. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Environmental Enteropathy
What is being tested?
VSL#3 and Capscan device
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
76 participants
Where
4 sitesin 4 countries
Study dates
1 Dec 2022to 30 Jun 2023
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Women over the age of 18 years in the second trimester of pregnancy, living in defined geographical areas of Bangladesh, Pakistan, Senegal and Zambia, where it can be assumed that environmental enteropathy is universal.

Who cannot join

  • Potential participants will not be enrolled if they:
  • have had diarrhoea, defined as the passage of three or more loose stools per 24 hours, in the preceding 14 days;
  • have taken antibiotics or probiotics in the preceding 14 days;
  • have taken non-steroidal anti-inflammatory drugs in the preceding 14 days;
  • have haemoglobin concentration <8g/dl;
  • have any illness which in the opinion of the investigator will complicate assessment of safety or efficacy;
Show all 9Show fewer
  • have any gastrointestinal contraindication to ingestion of a capsule (known or suspected gastrointestinal obstruction, stricture, fistula, gastroparesis, or any swallowing disorder);
  • have a plan to leave the study area within the follow-up period;
  • but may be enrolled if/when these disqualifiers have expired.

Trial locations and contacts

4 sites in 4 countries.

Miyoba Chipunza, MBA contact

973372863 ext. +260

miyoba@tropgan.net

4 sites in 4 countries

Bangladesh1 site
  • Icddr,B

    Dhaka, 1000

    Tafsir Dr Hasan, Dr, 1709651470 ext. +880, tafsir.hasan@icddrb.org

    Tahmeed Dr Ahmed, Dr

Other trials in Bangladesh

Pakistan1 site
  • Aga Khan University, icddr,b

    Karachi, Sindh, 75700

    Sheraz Ahmed, coordinator, 334-3131087 ext. +92, sheraz.ahmed@aku.edu

    Fyezah Dr Jehan, Dr

Other trials in Pakistan

Senegal1 site
  • Institut pasteur de dakar

    Dakar, 10200

    Ndeye Dr drame, Dr, 775513542 ext. +221, ndeyedieynaba.drame@pasteur.sn

    Yakhya Dieye, Dr

Other trials in Senegal

Zambia1 site
  • TROPGAN

    Lusaka, 10101

    Miyoba Chipunza, MBA, 973372863 ext. +260, miyoba@tropgan.net

    Prof Paul Kelly, DR, 966751875 ext. +260, m.p.kelly@qmul.ac.uk

Other trials in Zambia

About this study

This trial will determine if a well-established probiotic, Vivomixx, can modulate the maternal microbiota and ameliorate the maternal environmental enteropathy which compromises growth in the first 1000 days. The probiotic Vivomixx has been used in many thousands of people including pregnant women, both within and outside a research context. This trial is the first in a proposed series of proof-of-concept intervention studies which are intended to provide data to enable a rational selection of interventions to be evaluated at scale in future large scale phase 2 trial in which birth outcomes and postnatal growth will be key endpoints.

Read the detailed description

Stunting in young children refers to attenuated linear growth1. In the year 2020, 149.2 million children under the age of 5 years of age were stunted, accounting for 22% of stunting globally2. Stunting has short- and long-term consequences of increased morbidity and mortality3,4, impairment of neurocognitive development5 , impaired responses to oral vaccines6,7, and increased risk of non-communicable diseases. Stunting is partly driven by Environmental Enteric Dysfunction (EED), an enteropathic condition characterised by altered gut permeability, infiltration of immune cells and changes in villous architecture and cell differentiation8,9. EED may help explain why nutritional supplementation either during pregnancy or early childhood has minimal value in correcting childhood stunting10,11 Indeed, EED is believed to be responsible for 40% of childhood stunting12. Disruption in intestinal barrier function affects gut immune homeostasis, nutrient flows, and consequently dysbiosis in the gut microbiome. The gut microbiota consists of 100 trillion bacteria which interact with epithelial cells, the mucus layer and the mucosal immune system that balances tolerance and effector functions. Thus the gut microbiome has an important role in shaping the responsiveness of the gut immune system13. The mucus barrier and the normal gut microbiota limit enteropathogen colonisation. Influx of bacteria from the lumen to the systemic circulation represents microbial translocation and initiation of systemic of inflammatory process through recognition of pathogen-associated molecular patterns (PAMPs) by Pattern Recognition Receptors (PRRs) present on Antigen Presenting Cells (APCs). Three fundamental processes drive the epithelial damage which is so important in EED: infection, undernutrition, and immune dysfunction. Multiple clinical trials show that efforts to correct malnutrition through conventional therapies and improving hygiene and sanitation do not overcome growth deficits by more than about 10%10,11. There is increasing interest in the use of probiotics which may allow pathogen decolonization, improve barrier function and restore overall gut homeostasis. Such therapies are at early stage of trials but may have potential in addressing the global burden of EED, by improving barrier function and gut pathophysiology.

Colonization of gut by enteropathogens is common in children with EED. These include ETEC, Campylobacter, Shigella and Salmonella species. Consistent data from Bangladesh and Zambia show that children with refractory stunting carry over four pathogens on average, whilst controls carry less than two14,15. There is also clear evidence of altered composition of the microbiota in children with EED16,17,18.

Probiotics may serve to overcome the problem of EED through all mechanisms of pathogenicity, by providing additional bacteria that may help in intestinal decolonization of pathogenic microorganisms (changing the microbiological niche), promoting epithelial healing, improving nutrient absorption, and restoration of an appropriate immune balance between tolerance and responsiveness.

To date the focus of research on childhood stunting has been on the young child. It is increasingly appreciated, however, that stunting often begins in utero and the focus has shifted to women's health and pregnancy. For example, the Lancet 2021 Series on maternal and child undernutrition states that "Investments to reduce undernutrition in women are important not only for women's own health but also for the health and nutrition of their children"19. Results from rural Bangladesh reveal poor gestational weight gain that ultimately leads to intrauterine growth restriction, low birth weight and ultimately stunting and wasting20,21. Furthermore, another study recently completed in slum settlements of Dhaka, Bangladesh demonstrated a high prevalence of EED among undernourished women. Intestinal histopathology was abnormal in more than 80% of women22. We postulate that growth retardation in utero is a consequence of EED in the mother during pregnancy and lactation. This leads to systemic inflammation, which leads to disadvantageous partitioning of nutrients, and reduced nutrient availability.

This trial will explore the conceptual framework that a well known probiotic, that can improve the composition of the gut microbiota, can also reduce biomarkers of intestinal inflammation and gut health. This will restore healthy microbial signalling to the host epithelium, ameliorate barrier function through secretion of mucus and antimicrobial factors, and improve nutrient availability.

Being tested
VSL#3, Capscan device, Placebo

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • VSL#3Dietary supplement

    Also called Vivomixx

    VSL#3 is a commercial probiotic mixture consisting of eight probiotic lactic acid bacteria and Bifidobacteria including Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus casei, Lactobacillus delbrueckii subspecies bulgaricus, Streptococcus salivarius subspecies thermophiles, Bifidobacterium breve, Bifidobacterium longum, and Bifidobacterium infantis. VSL#3 contributes to balancing the gut and vaginal microbiota and is used as a food supplement for management of diseases like irritable bowel syndrome, ulcerative colitis or ileal pouch.

  • Capscan deviceDevice

    Also called capstan

    The CapScan device is a short-term single-use class IIa ingestible medical device that collects fluids from the gastrointestinal ("GI") tract and is collected in the stool. GI samples are then extracted from the device and analyzed outside the body.

  • PlaceboCombination product

    microcrystalline cellulose

Study groups in NCT05608928
Study groupRoleWhat they receive
VivomixxExperimentalVivomixx also known as VSL#3 is a commercial probiotic mixture consisting of eight probiotic lactic acid bacteria and Bifidobacteria including Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus casei, Lactobacillus delbrueckii subspecies bulgaricus, Streptococcus salivarius subspecies thermophiles, Bifidobacterium breve, Bifidobacterium longum, and Bifidobacterium infantis. VSL#3 contributes to balancing the gut and vaginal microbiota and is used as a food supplement for management of diseases like irritable bowel syndrome, ulcerative colitis or ileal pouch.
Receives: Dietary Supplement: VSL#3; Device: Capscan device; Combination Product: Placebo
Capscan deviceExperimentalThe CapScan device is a short-term single-use class IIa ingestible medical device that collects fluids from the gastrointestinal ("GI") tract and is collected in the stool. GI samples are then extracted from the device and analyzed outside the body.
Receives: Dietary Supplement: VSL#3; Device: Capscan device; Combination Product: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage change (mean, unweighted) in a multiple panel of biomarkers between baseline and last sample collected after 56 days of treatment, compared to control group.

    Plasma CRP by ELISA Plasma AGP by ELISA Plasma sCD14 by ELISA Plasma LBP by ELISA Plasma iFABP by ELISA Plasma CD163 by ELISA Faecal MPO by ELISA Faecal neopterin by ELISA Faecal calprotectin by ELISA Faecal lipocalin by ELISA

    Measured: 2 months

Secondary outcomes (6)
  1. Reduction in colonisation

    Stool qPCR for Salmonella, Shigella, Campylobacter, ETEC, EPEC, EAEC, rotavirus, norovirus, Giardia and Cryptosporidium

    Measured: 2 Months

  2. Change in microbiome

    Whole genome shotgun metagenomics sequencing (MetaPhlAn) in faecal and CAPSCAN samples

    Measured: 2 months

  3. Reduction in LR ratio in Vivomixx compared to placebo groups

    LR ratio in 3 hour/120 min urine collections following dose of 5g lactulose and 1g rhamnose

    Measured: 2 months

  4. Change in metabolome

    Untargeted urine and plasma (and fecal) metabolome before and after intervention

    Measured: 2 months

  5. Weight gain velocity in the 2nd trimester of pregnancy

    Rate of weight gain (kg/week)

    Measured: weekly for 56 days

  6. Measurements of variability, including standard deviations and kappa values

    Preliminary work across all sites using identical kits and harmonised SOPs

    Measured: 2 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Nov 2022
  2. Study start1 Dec 2022 (estimated)
  3. Primary completion30 May 2023 (estimated)
  4. Study completion30 Jun 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Single group
Model description
Multi-site phase II randomised controlled trial
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
76 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05608928
Sponsor's protocol ID
NHRA000014/18/07/2022
Acronym
EMP
Status last verified
Nov 2022
First submitted
1 Nov 2022
Last updated
8 Nov 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
Yes
Individual data sharing
Undecided

Publications

  • Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, Ezzati M, Grantham-McGregor S, Katz J, Martorell R, Uauy R; Maternal and Child Nutrition Study Group. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013 Aug 3;382(9890):427-451. doi: 10.1016/S0140-6736(13)60937-X. Epub 2013 Jun 6.

    PubMed 23746772
  • Olofin I, McDonald CM, Ezzati M, Flaxman S, Black RE, Fawzi WW, Caulfield LE, Danaei G; Nutrition Impact Model Study (anthropometry cohort pooling). Associations of suboptimal growth with all-cause and cause-specific mortality in children under five years: a pooled analysis of ten prospective studies. PLoS One. 2013 May 29;8(5):e64636. doi: 10.1371/journal.pone.0064636. Print 2013.

    PubMed 23734210
  • Prendergast AJ, Humphrey JH. The stunting syndrome in developing countries. Paediatr Int Child Health. 2014 Nov;34(4):250-65. doi: 10.1179/2046905514Y.0000000158. Epub 2014 Oct 13.

    PubMed 25310000
  • de Onis M, Branca F. Childhood stunting: a global perspective. Matern Child Nutr. 2016 May;12 Suppl 1(Suppl 1):12-26. doi: 10.1111/mcn.12231.

    PubMed 27187907

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing VSL#3 and Capscan device in people with Environmental Enteropathy, run by Tropical Gastroenterology & Nutrition Group (TROPGAN) at 4 sites in 4 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 8 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in Bangladesh, Pakistan, Senegal, Zambia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Miyoba Chipunza, MBA (973372863 ext. +260, miyoba@tropgan.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage change (mean, unweighted) in a multiple panel of biomarkers between baseline and last sample collected after 56 days of treatment, compared to control group. (time frame: 2 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05608928, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Nov 2022.

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