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Completed

NCT Number: NCT02188953

Evaluation of ACCS100 to Reduce Aflatoxin Exposure in Kenya

The purpose of this study is to pilot test the effectiveness, acceptability, and palatability of ACCS100 in a high-risk Kenyan population.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Makindu Health Center

Makindu, Kenya

About this study

Aflatoxins are harmful by-products of the molds Aspergillus flavus and A. parasiticus and are major contaminants of agricultural produce such as maize. Acute aflatoxin exposure (i.e., aflatoxicosis) can lead to jaundice, vomiting, abdominal pain, and liver failure, with documented fatality rates as high as 40%. Kenya experiences extreme aflatoxin exposure and fatal, recurring aflatoxicosis outbreaks. Numerous clinical trials have found heat processed calcium dioctahedral smectite clay [i.e., Air Classified Calcium Silicate (ACCS100)] to be safe and effective in binding to aflatoxin to decrease bioavailability and subsequently reduce toxin-induced effects. The investigators propose to pilot test the effectiveness, acceptability, and palatability of ACCS100 in a high-risk Kenyan population. If successful, ACCS100 could be scaled-up for use in Kenya to prevent aflatoxin-associated mortality during high-risk periods. To accomplish this objective, the investigators will recruit fifty health adults into a crossover study. Each participant will spend one week consuming ACCS100 and one week consuming a calcium carbonate placebo. Daily first morning void urine samples will monitor effectiveness in reducing aflatoxin bioavailability, and periodic questionnaires will assess acceptance and palatability.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult ≥18 years of age
  • Consumes corn- and/or peanut-derived foods at least four times per week
  • No plans to travel away from the household for more than one day in the next month

Exclusion criteria

  • Women who may be pregnant
  • History of medical illnesses
  • Presence of protein or glucose in urine using chemstrip
  • Does not provide informed consent

Treatment and study plan

ACCS100

Drug

ACCS100 is made from Hydrated Sodium Calcium Aluminosilicate, which is a substance generally recognized as safe by the U.S. FDA.

Other names: Air Classified Calcium Silicate

Calcium carbonate placebo

Drug

Primary outcomes

  1. Change from baseline of urine aflatoxin M1 levels

    Time frame: Daily during each study arm

    Urine samples will be collected at baseline (Day 0) and daily for seven days during Arm 1 (Days 1-7). Urine samples will also be collected at baseline (Day 13) and daily for seven days during Arm 2 (Days 13-19).

Secondary outcomes

  1. Serum aflatoxin B1-lysine adduct levels

    Time frame: Baseline of Arm 1 (Day 0) and end of arm 2 (Day 20)

    Baseline of Arm 1 (Day 0) and end of arm 2 (Day 20).

  2. Palatability questionnaire

    Time frame: End of arm 1 (Day 8) and end of arm 2 (Day 20)

    End of arm 1 (Day 8) and end of arm 2 (Day 20)

  3. Daily diary and adverse event reporting form

    Time frame: Daily during arm 1 (Days 2-8) and arm 2 (Days 14-20)

    Daily during arm 1 (Days 2-8) and arm 2 (Days 14-20)

  4. Acceptability questionnaire

    Time frame: End of arm 2 (Day 20)

    End of arm 2 (Day 20)

Sponsors and collaborators

Lead sponsor

Kenya Medical Research Institute

Other

Collaborators

  • Centers for Disease Control and Prevention
  • Kenya Ministry of Health
  • Texas A&M University

Registry information

Official study title

Evaluation of the Effectiveness, Acceptability, and Palatability of Air Classified Calcium Silicate (ACCS100) Clay to Reduce Aflatoxin Exposure in a High-risk Community in Kenya

Acronym: ACCS100

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jul 14, 2014
Registry last updated
Sep 16, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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